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salicylic acid and Anhidrotic Ectodermal Dysplasia

salicylic acid has been researched along with Anhidrotic Ectodermal Dysplasia in 181 studies

Scalp: The outer covering of the calvaria. It is composed of several layers: SKIN; subcutaneous connective tissue; the occipitofrontal muscle which includes the tendinous galea aponeurotica; loose connective tissue; and the pericranium (the PERIOSTEUM of the SKULL).

Research Excerpts

ExcerptRelevanceReference
"In hyperthyroidism-complicated pregnancies, medical therapy is necessary to reach an euthyroid condition, and propylthiouracil (PTU) or methimazole (MMI) are used."3.72Malformations following methimazole exposure in utero: an open issue. ( Blaid, D; Divizia, MT; Ferraris, S; Ferrero, GB; Lerone, M; Nemelka, O; Rosaia, L; Silengo, M; Valenzise, M, 2003)
"Two neonates with composite type aplasia cutis congenita are described as examples of this disorder, and their management, including complications, is discussed."2.53Aplasia Cutis Congenita of the Scalp, Composite Type: The Criticality and Inseparability of Neurosurgical and Plastic Surgical Management. ( Ketch, LL; Winston, KR, 2016)
"Now, he is 3 years old, and has microcephaly, moderate mental retardation, left spastic hemiplegia, and epilepsy."2.41A case of Adams-Oliver syndrome associated with acrania, microcephaly, hemiplegia, epilepsy, and mental retardation. ( Caksen, H; Kurtoğlu, S, 2000)
"Aplasia cutis congenita is a heterogeneous disorders group with a rare reported incident of 0."1.91Aplasia Cutis Congenita of the Scalp with Bone Defect and Exposed Sagittal Sinus in Trisomy 13 Newborn - a Case Report. ( Abdulwahab, AH; Al Nefily, RM; Al-Shammari, AA; AlAnazi, RA; AlMatrifi, FR; Ammar, AS, 2023)
"We diagnosed aplasia cutis congenita, a rare disorder with a wide variation in clinical symptoms."1.72[A child with a bald spot on her scalp]. ( de Jong, N; Janse, I, 2022)
"Membranous aplasia cutis congenita (MACC) presents at birth characterized by oval epidermis defect."1.72Dermoscopic characteristics of membranous aplasia cutis congenita: Report of 56 cases. ( Jiang, HJ; Li, YD; Pu, YJ; Shu, H; Zhang, L; Zhang, Z, 2022)
"The sister had microcephaly, periventricular calcifications, minor retinal vasculopathy, and mild impaired neurodevelopment, but only very subtle limb abnormalities and no ACC."1.72Intrafamilial phenotypic variability in autosomal recessive DOCK6-related Adams-Oliver syndrome. ( Aguirre-Guillén, RL; Bobadilla-Morales, L; Corona-Rivera, A; Corona-Rivera, JR; Pacheco-Torres, PA; Peña-Padilla, C; Quezada-Salazar, CA; Rivera-Montellano, ML; Schanze, D; Schanze, I; Zenker, M; Zepeda-Romero, LC, 2022)
"The clinical diagnosis is Aplasia Cutis Congenita."1.62[An infant with multiple lesions of the scalp]. ( Boudewijns, K; Eijkemans, M; Verberne, L, 2021)
"ACC represents a congenital scarring alopecia with permanent loss of skin appendages."1.56Aplasia cutis congenita of the scalp: Histopathologic features and clinicopathologic correlation in a case series. ( Bösmüller, H; Gassenmaier, M; Metzler, G, 2020)
"The most common location of the aplasia cutis congenita lesion was the vertex scalp (49."1.56Low risk of clinically important central nervous system dysraphism in a cohort study of 69 patients with isolated aplasia cutis congenita of the head. ( Humphrey, SR; Kuemmet, TJ; Lew, SM; Maheshwari, M; Michalik, D; Miller, JJ, 2020)
"Bullous aplasia cutis congenita (BACC) is a rare clinical subtype that has few documented reports in the literature."1.56Bullous aplasia cutis congenita: A rare presentation of a rare disease. ( Watchmaker, J; Watchmaker, L, 2020)
"ACC is associated with chromosomal abnormalities and 35-50 percent of the time with trisomy 13 (Patau syndrome)."1.56Multiple Aplasia Cutis Congenita Lesions of the Scalp: A Case Study. ( Whalen, M, 2020)
"Aplasia cutis congenita is a rare but heterogeneous group of conditions characterized by the absence of one or more areas of skin sometimes extending to deeper tissues."1.56Pseudo-cobra neck deformity due to aplasia cutis congenita. ( Davison, WL; Feit, NZ; Modi, VK; Sclafani, AP, 2020)
"We report two cases of aplasia cutis congenita associated with hair collar signs and hemangioma simplex in their parietal regions."1.51Two cases of aplasia cutis congenita with hair collar signs and macrophage hyperplasia. ( Harada, A; Ikura, Y; Seto, H; Takayama, E, 2019)
"Aplasia Cutis Congenita is a rare disorder with circumscribed, partial or widespread absence of skin and subcutaneous soft tissue; in about 20% it also causes skull defects."1.46APLASIA CUTIS CONGENITA TYPE I - A CASE SERIES. ( Chokoeva, A; Handjani, F; Tchernev, G; Verma, S; Wollina, U, 2017)
"We report a rare case of EPDS after aplasia cutis congenita in a child."1.46Erosive pustular dermatosis of the scalp after aplasia cutis congenita in a 9-year-old patient: A 5-year follow-up. ( Cadore de Farias, D; Fertig, R; Maddy, A; Rigatti, M; Simão Corrêa Filho, S; Tosti, A, 2017)
"Aplasia cutis congenital is a rare condition presenting with localized or widespread congenital absence of skin, most commonly affecting the scalp."1.43Technique for Management of Aplasia Cutis Congenita of the Scalp With a Skin Allograft. ( Burge, J; Lonie, S; Phua, Y, 2016)
"Aplasia cutis congenita is a rare congenital disorder characterised by the absence of skin."1.43[Aplasia cutis congenita]. ( Rath, T; Steinbacher, J; Tzou, CH, 2016)
"Aplasia cutis congenita is a rare, congenital disorder."1.40Aplasia cutis congenita: clinical management and a new classification system. ( Berezovsky, AB; Krieger, Y; Landau, D; Levy, A; Pagkalos, VA; Rosenberg, L; Shoham, Y; Silberstein, E; Silberstein, T, 2014)
"Aplasia cutis congenita is a rare anomaly presenting with the absence of skin."1.39A rare case of aplasia cutis congenita. ( Dahmardehei, M, 2013)
"Aplasia cutis congenita is a rare scalp defect with occasional absence of underlying bone and dura."1.38Reconstruction of complex aplasia cutis congenita. ( Bui, CJ; Singh, M; St-Hilaire, H, 2012)
"Coexistence of isolated preaxial polydactyly without terminal extremity defect and ACC is extremely rare."1.37Autosomal dominant aplasia cutis in three generations and one case with preaxial polydactyly in the last generation. ( Balci, S; Büyük, S; Çağlar, K; Yağci-Küpeli, B, 2011)
"Aplasia cutis congenita is a rare congenital condition characterised by the absence of some or all layers of the skin."1.36Aplasia cutis congenita. A case of scalp defect repair using two opposing bipedicled local flaps. ( Carter, M; O'Neill, JK; Warr, RP, 2010)
"Adams-Oliver syndrome is a rare congenital disorder that includes congenital scalp and skull defects, variable degrees of terminal transverse limb anomalies, and cardiac malformations."1.35Management of large scalp and skull defects in a severe case of Adams-Oliver syndrome. ( Fried, A; Khashab, ME; Khashab, YE; Nejat, F; Pierce, SD; Rhee, ST, 2009)
"Of approximately 200 different ectodermal dysplasias, about 30 have been identified at molecular level with identification of the causative gene."1.35Rationale and background as basis for a new classification of the ectodermal dysplasias. ( Itin, PH, 2009)
"Adams-Oliver syndrome has a wide spectrum of anomalies ranging from aplasia cutis congenita, cutis marmorata telangiectatica congenita and transverse limb defects to lethal anomalies."1.35Aplasia cutis congenita of the scalp, skull and dura associated with Adams-Oliver syndrome. ( Akalan, N; Bahadir, S; Bilginer, B; Onal, MB, 2008)
"Aplasia cutis congenita is a rare disorder characterized by absence of skin."1.35Aplasia cutis congenita: management of a large skull defect with acrania. ( Cavalheiro, S; Dutra, LB; Ferreira, LM; Kreniski, TM; Pereira, MD; Zanon, N, 2009)
"The National Foundation for Ectodermal Dysplasias convened the International Research Symposium for AEC Syndrome on November 8-10, 2006, at Texas Children's Hospital/Baylor College of Medicine, Houston, TX with appropriate IRB approval."1.35Dermatologic findings of ankyloblepharon-ectodermal defects-cleft lip/palate (AEC) syndrome. ( Bree, AF; Julapalli, MR; Scher, RK; Siegfried, EC; Sybert, VP, 2009)
"Aplasia cutis congenita is a rare congenital disorder of skin and most commonly involves the scalp."1.34Aplasia cutis congenita of the scalp and calvarium: conservative wound management with novel wound dressing materials. ( Bağdatoğlu, C; Başterzi, Y; Demirkan, F; Sari, A, 2007)
"Aplasia cutis congenita is a special condition, with local vascular abnormalities: local flaps are prohibited."1.33[Scalp surgery in children: principles and therapeutic aspects]. ( Buis, J; Delbecque, M; Franchi, G; Picard, A; Sergent, B; Vazquez, MP, 2005)
"Aplasia cutis congenita is a rare condition characterized by the absence of skin layers."1.32[Large scalp and skull defect in patient with aplasia cutis congenita]. ( Giannetti, AV; Henriques, JG; Henriques, KS; Pianetti Filho, G, 2004)
"Aplasia cutis congenita is a rare disorder characterized by developmental absence of skin on the scalp as multiple or solitary, noninflammatory, well demarcated, oval or circular 1- to 2-cm ulcers."1.31Our experience with aplasia cutis congenita. ( Caksen, H; Kurtoglu, S, 2002)
"Cutis aplasia (or aplasia cutis congenita) is a congenital absence of all skin layers, often extending through bone."1.31Complete osseous regeneration of a large skull defect in a patient with cutis aplasia: a conservative approach. ( Buchman, SR; Colville, C; Muraszko, K; Rhee, ST, 2002)
"Aplasia cutis congenita is a rare condition characterized by the congenital absence of skin."1.31Surgical treatment of aplasia cutis congenita of the scalp associated with bilateral coronal synostosis. ( Arai, H; Ichida, M; Inoue, M; Komuro, Y; Miyajima, M; Sato, K; Seno, H; Yanai, A, 2002)
"Aplasia cutis congenita is a condition that can present with a wide variety of symptoms and many attempts have been made to classify it comprehensively."1.31Aplasia cutis congenita associated with a lipoma. ( Moss, AL; Uppal, RS, 2000)
"Some patients had partial syndactyly of the 3rd and 4th fingers, and complete cutaneous syndactyly of the 2nd and 3rd toes."1.29Scalp-ear-nipple syndrome: additional manifestations. ( Edwards, MJ; McDonald, D; Moore, P; Rae, J, 1994)
"Hay-Wells syndrome is an autosomal dominant condition characterized by ankyloblepharon filiforme adnatum, ectodermal dysplasia, and cleft palate with or without associated cleft lip (AEC syndrome)."1.29Severe skin erosions and scalp infections in AEC syndrome. ( Stephan, MJ; Sybert, VP; Vanderhooft, SL, 1993)
"Rapp-Hodgkin syndrome is an autosomal dominant condition characterized by cleft lip and palate, peculiar craniofacial features, and ectodermal dysplasia, consisting of abnormalities of teeth, hair, nails and sweating."1.29Rapp-Hodgkin syndrome and AEC syndrome: are they the same entity? ( Barbareschi, M; Cambiaghi, S; Caputo, R; Menni, S; Tadini, G, 1994)
"A case of aplasia cutis congenita of the scalp with bony defect in a newborn treated by early excision and reconstruction is presented."1.28Scalp aplasia cutis congenita: closure by the L-shaped flap. ( Attalla, MF; el-Sayed, AM, 1992)
"We report on the association of aplasia cutis congenita (ACC) in the midline of the scalp vertex and coarctation of the aorta (CA) in mother and son."1.28Familial aplasia cutis congenita and coarctation of the aorta. ( Dallapiccola, B; Digilio, C; Giannotti, A; Marino, B; Obregon, G, 1992)
"Nine patients with aplasia cutis congenita were treated in our department during the past 30 years."1.28Large skull defect in aplasia cutis congenita treated by pericranial flap: long-term follow-up. ( Berger, J; Govrin, J; Moscona, R, 1991)

Research

Studies (181)

TimeframeStudies, this research(%)All Research%
pre-199020 (11.05)18.7374
1990's21 (11.60)18.2507
2000's47 (25.97)29.6817
2010's57 (31.49)24.3611
2020's36 (19.89)2.80

Authors

AuthorsStudies
Boudewijns, K1
Verberne, L1
Eijkemans, M1
Rojnueangnit, K1
Phawan, T1
Khetkham, T1
Techasatid, W1
Sirichongkolthong, B1
Ngeow, A1
Hui, C1
Chua, AWC1
Koh, M1
Ong, YS2
Poon, WB1
Tripodi, GD1
Dickerman, DI1
LeMosy, EK1
Davis, LS1
Okido, MM1
Ragazini, CS1
Duarte, G1
Coutinho, CM1
Marcolin, AC1
Jiang, Y1
Yu, X1
Deng, MG1
Wu, CX1
Xu, XY1
Luo, T1
Zhang, ZJ1
de Jong, N1
Janse, I1
Gagliani, EK1
Gutzwiller, LM1
Kuang, Y1
Odaka, Y1
Hoffmeister, P1
Hauff, S1
Turkiewicz, A1
Harding-Theobald, E1
Dolph, PJ1
Borggrefe, T1
Oswald, F1
Gebelein, B1
Kovall, RA1
Zhang, L1
Zhang, Z1
Jiang, HJ1
Pu, YJ1
Shu, H1
Li, YD1
Lukas, ML1
Harald, G1
Sanz, J1
Trippel, M1
Sabina, G1
Jochen, R1
Cospain, A1
Rivera-Barahona, A1
Dumontet, E1
Gener, B1
Bailleul-Forestier, I1
Meyts, I1
Jouret, G1
Isidor, B1
Brewer, C1
Wuyts, W3
Moens, L1
Delafontaine, S1
Keung Lam, WW1
Van Den Bogaert, K1
Boogaerts, A1
Scalais, E1
Besnard, T1
Cogne, B1
Guissard, C1
Rollier, P1
Carre, W1
Bouvet, R1
Tarte, K1
Gómez-Carmona, R1
Lapunzina, P1
Odent, S1
Faoucher, M1
Dubourg, C1
Ruiz-Pérez, VL1
Devriendt, K2
Pasquier, L1
Pérez-Jurado, LA1
Zepeda-Romero, LC1
Zenker, M3
Schanze, D2
Schanze, I1
Peña-Padilla, C2
Quezada-Salazar, CA1
Pacheco-Torres, PA1
Rivera-Montellano, ML1
Aguirre-Guillén, RL2
Bobadilla-Morales, L2
Corona-Rivera, A2
Corona-Rivera, JR2
Quak, SM1
Chong, SY1
Moreno-Casas, G1
Pereira-González, A1
Rodríguez-Nevado, I1
Narváez-Moreno, B1
Chaves-Álvarez, A1
Peral-Rubio, F1
Zaersabet, M1
Koochakkhani, S1
Sarmast, Y1
Salmani, H1
Errichetti, E1
Hui, CLY1
Ngeow, AJH1
Ang, DSY1
AlMatrifi, FR1
Al-Shammari, AA1
Al Nefily, RM1
AlAnazi, RA1
Abdulwahab, AH1
Ammar, AS1
Gassenmaier, M1
Bösmüller, H1
Metzler, G1
Yang, MY1
Ha, DL1
Kim, HS1
Ko, HC1
Kim, BS1
Kim, MB1
Kuemmet, TJ1
Miller, JJ1
Michalik, D1
Lew, SM1
Maheshwari, M1
Humphrey, SR1
Watchmaker, L1
Watchmaker, J1
Whalen, M1
Sathishkumar, D1
Ogboli, M1
Moss, C1
Naravane, AV1
Belin, PJ1
Bhambhani, V1
Quiram, PA1
Silva Díaz, E1
Molini Menchón, MO1
Estébanez Corrales, A1
Garcia-Vázquez, A1
Estañ Capell, J1
Sáez-Martín, L1
Martín Hernández, J1
Feit, NZ1
Davison, WL1
Sclafani, AP1
Modi, VK1
Schnabel, F1
Kamphausen, SB1
Funke, R1
Kaulfuß, S1
Wollnik, B1
Davis, MJ1
Voller, LM1
Gonzalez, SR1
Abu-Ghname, A1
Davies, LW1
Bedwell, JR1
Lee, GL1
Hunt, RD1
Phung, TL1
Buchanan, EP1
Souissi, A1
Ben Lagha, I1
Mama, M1
Chelly, I1
Haouet, S1
Mokni, M1
Mushtaq, S1
Nofal, A1
Tahara, J1
Dainichi, T1
Kaku, Y1
Kataoka, T1
Kishimoto, H1
Kogame, T1
Kabashima, K1
Scotti, A1
Benanti, E1
Augelli, F1
Baruffaldi Preis, FW1
Ugowe, OJ1
Balogun, SA1
Adejuyigbe, EA1
Butler, KM1
Bahrambeigi, V1
Merrihew, A1
Friez, MJ1
Cathey, SS1
Wollina, U1
Chokoeva, A1
Verma, S1
Tchernev, G1
Handjani, F1
Perry, BM1
Maughan, CB1
Crosby, MS1
Hadenfeld, SD1
Sezgin, B1
Sibar, S1
Findikcioglu, K1
Sencan, A1
Emmez, H1
Baykaner, K1
Ozmen, S1
Miyagawa, T1
Kadono, T1
Saigusa, R1
Numajiri, H1
Omatsu, J1
Funamizu, K1
Yamada, D1
Masui, Y1
Asano, Y1
Sato, S1
Fertig, R1
Maddy, A1
Cadore de Farias, D1
Simão Corrêa Filho, S1
Rigatti, M1
Tosti, A1
Park, ES1
Park, JH1
Shin, HS1
Nam, SM1
Chen, HY1
Hsieh, WS1
Abusamra, A1
Dharia, D1
Aleshaki, J1
Meester, JAN1
Sukalo, M1
Schröder, KC1
Baynam, G1
Borck, G1
Bramswig, NC1
Duman, D1
Gilbert-Dussardier, B1
Holder-Espinasse, M1
Itin, P1
Johnson, DS1
Joss, S1
Koillinen, H1
McKenzie, F1
Morton, J1
Nelle, H1
Reardon, W1
Roll, C1
Salih, MA1
Savarirayan, R1
Scurr, I1
Splitt, M1
Thompson, E1
Titheradge, H1
Travers, CP1
Van Maldergem, L1
Whiteford, M1
Wieczorek, D1
Vandeweyer, G1
Trembath, R1
Van Laer, L1
Loeys, BL1
Southgate, L1
Ambooken, B1
Kesavan, A1
Neelakandan, A1
Mathew, A1
Kamat, D1
Sendhil Kumaran, M1
Torkamand, F1
Ayati, A1
Habibi, Z1
Nejat, F2
Takayama, E1
Harada, A1
Ikura, Y1
Seto, H1
Russo, F1
Zenteno, JC1
Pelcastre-Luna, E1
Miguel-Jiménez, K1
Cabral-Macías, J1
Anderson, SM1
Marneros, AG2
Beck, AE1
Turner, EH1
McMillin, MJ1
Edwards, MJ2
Field, M1
de Macena Sobreira, NL1
Perez, AB1
Fortes, JA1
Lampe, AK1
Giovannucci Uzielli, ML1
Gordon, CT1
Plessis, G1
Le Merrer, M1
Amiel, J1
Reichenberger, E1
Shively, KM1
Cerrato, F1
Labow, BI1
Tabor, HK1
Smith, JD1
Shendure, J1
Nickerson, DA1
Bamshad, MJ1
Dahmardehei, M1
Yin, HY1
Tang, XJ1
Liu, W1
Shi, L1
Yin, L1
Yang, B1
Ma, JG1
Zhang, ZY1
Kutlubay, Z1
Pehlivan, Ö1
Rostami, P1
Mahmoudi, E1
Sotoudeh, A1
Nakhaeimoghadam, M1
Lurkin, I1
Zwarthoff, EC1
Rezaei, N1
Isrie, M1
Van Esch, H1
Iftikhar, N1
Ahmad Ghumman, FI1
Janjua, SA1
Ejaz, A1
Butt, UA1
Bassi, A1
Greco, A1
de Martino, M1
Silberstein, E1
Pagkalos, VA1
Landau, D1
Berezovsky, AB1
Krieger, Y1
Shoham, Y1
Levy, A1
Rosenberg, L1
Silberstein, T1
Johnson, R1
Offiah, A1
Cohen, MC1
Marcovici, I1
Betancourth-Alvarenga, JE1
Vázquez-Rueda, F1
Vargas-Cruz, V1
Paredes-Esteban, RM1
Ayala-Montoro, J1
Peacock, JD1
Dykema, KJ1
Toriello, HV1
Mooney, MR1
Scholten, DJ1
Winn, ME1
Borgman, A1
Duesbery, NS1
Hiemenga, JA1
Liu, C1
Campbell, S1
Nickoloff, BP1
Williams, BO1
Steensma, M1
Ntumba-Tshitenge, O1
Kaputu-Kalala-Malu, C1
Mukampunga, C1
Mukendi, KM1
Maeda, T1
Oyama, A1
Funayama, E1
Furukawa, H1
Cho, K1
Yamamoto, Y1
Puvabanditsin, S1
February, M1
Garrow, E1
Bruno, C1
Mehta, R1
Madan, A1
Sardana, K1
Garg, VK1
Mericli, AF1
Chen, K1
Murariu, D1
Jane, JA1
Lin, KY1
Gencel, E1
Eser, C1
Tabakan, I1
Kesiktas, E1
Yavuz, M1
Winston, KR1
Ketch, LL1
Lonie, S1
Phua, Y1
Burge, J1
Hadad, I1
Meara, JG1
Rogers-Vizena, CR1
Steen, AJ1
Shin, JH1
Pace, NC1
Edgar, M1
Clay, MR1
Linos, K1
Barton, DT1
Mann, JA1
Hayashi, R1
Abe, R1
Shimomura, Y1
Steinbacher, J1
Rath, T1
Tzou, CH1
Pimenta, J1
Lapa, P1
Ramos, L1
Bilginer, B1
Onal, MB1
Bahadir, S1
Akalan, N1
Silva, JC1
Almeida, JP1
Serra, S1
Faquini, I1
Quinino, S1
Magalhães, FN1
Azevedo-Filho, H1
Itin, PH1
O'Neill, JK1
Carter, M1
Warr, RP1
Dutra, LB1
Pereira, MD1
Kreniski, TM1
Zanon, N1
Cavalheiro, S1
Ferreira, LM1
Bree, AF2
Julapalli, MR1
Scher, RK1
Sybert, VP3
Siegfried, EC1
Khashab, ME1
Rhee, ST2
Pierce, SD1
Khashab, YE1
Fried, A1
Zhou, J1
Zheng, L1
Tao, W1
Yéo, S1
Perrot, P1
Bellier-Waast, F1
David, A1
Duteille, F1
Messerer, M1
Diabira, S1
Belliard, H1
Hamlat, A1
Tröbs, RB1
Barenberg, K1
Hemminghaus, M1
Günther, M1
Neid, M1
Alexiou, G1
Sfakianos, G1
Prodromou, N1
Bharti, G1
Groves, L1
David, LR1
Sanger, C1
Argenta, LC1
Blyth, M1
Baralle, D1
Cho, AY1
Lee, SS1
Lee, Y1
Kim, CD1
Lee, JH1
Seo, YJ1
Blouin, MM1
Bernard, J1
Caron, F1
Auger, I1
Yağci-Küpeli, B1
Çağlar, K1
Büyük, S1
Balci, S1
Singh, M1
Bui, CJ1
St-Hilaire, H1
Harvey, G1
Solanki, NS1
Anderson, PJ1
Carney, B1
Snell, BJ1
Udayakumaran, S1
Mathew, J1
Panikar, D1
Sheckter, C1
Rommer, E1
Francis, C1
Block, V1
Chen, J1
Rizvi, M1
Urata, MM1
Hammoudeh, J1
Caksen, H2
Kurtoglu, S2
Colville, C1
Buchman, SR1
Muraszko, K1
Komuro, Y1
Yanai, A1
Seno, H1
Ichida, M1
Inoue, M1
Miyajima, M1
Arai, H1
Sato, K1
Jabbar, A1
Djoudi, D1
de Kleine, MJ1
Saraiya, HA1
Bajpai, M1
Pal, K1
Plottova-Puech, I1
Vidal, C1
Godard, W1
Cambazard, F1
Ribuffo, D1
Costantini, M1
Gullo, P1
Houseman, ND1
Taylor, GI1
WEINBERG, A1
GITTELSON, S1
CONWAY, H2
JOHNSON, G2
WALKER, JC1
KOENIG, JA1
IRWIN, L1
MEIJER, R1
HODGMAN, JE1
MATHIES, AW1
LEVAN, NE1
JOHNSONBAUGH, RE1
LIGHT, IJ1
SUTHERLAND, JM1
Ferraris, S1
Valenzise, M1
Lerone, M1
Divizia, MT1
Rosaia, L1
Blaid, D1
Nemelka, O1
Ferrero, GB1
Silengo, M1
Urbani, CE1
Rouse, C1
Siegfried, E1
Breer, W1
Nahass, G1
Sinha, A1
Sarin, YK1
Henriques, JG1
Pianetti Filho, G1
Giannetti, AV1
Henriques, KS1
Sammartino, G1
Marenzi, G1
Colella, G1
Califano, L1
Grivetto, F1
Mortellaro, C1
Perlyn, CA1
Schmelzer, R1
Govier, D1
Marsh, JL1
Ploplys, EA1
Muzaffar, AR1
Gruss, JS1
Ellenbogen, RG1
Azad, S1
Falder, S1
Harrison, J1
Graham, K1
Smith, VV1
Anderson, G1
Malone, M1
Sebire, NJ1
Jones, CH1
Andrews, C1
Picard, A1
Franchi, G1
Delbecque, M1
Sergent, B1
Buis, J1
Vazquez, MP1
Vanamo, K1
Härmä, M1
Tosun, Z1
Ozkan, A1
Savaci, N1
Santos de Oliveira, R1
Barros Jucá, CE1
Lopes Lins-Neto, A1
Aparecida do Carmo Rego, M1
Farina, J1
Machado, HR1
Lahiri, A1
Nishikawa, H1
Gan, YC1
Steinbok, P1
Shivakumar, SK1
Dwarakanath, S1
Swaroop, G1
Venkataramana, NK1
Başterzi, Y1
Bağdatoğlu, C1
Sari, A1
Demirkan, F1
Rodrigues, RG1
Heras Mulero, C1
Bartralot Soler, R1
Rodríguez-Cano, L1
Mollet Sánchez, J1
Palacio Aller, L1
Aparicio Español, G1
Bodet Castillo, D1
Bassas Freixas, P1
García-Patos, V1
Aloulou, H1
Chaari, W1
Khanfir, S1
Zroud, N1
Kammoun, TH1
Abdelmoula, M1
Hachicha, M1
Drolet, B1
Prendiville, J1
Golden, J1
Enjolras, O1
Esterly, NB1
Blume-Peytavi, U1
Gollnick, HM1
Föhles, J1
Kremer, G1
Pineda, MS1
Phan, KH1
Orfanos, CE2
Theile, RJ1
Lanigan, MW1
McDermant, GR1
McDonald, D1
Moore, P1
Rae, J1
Fryburg, JS1
Greer, KE1
Vanderhooft, SL1
Stephan, MJ1
Cambiaghi, S1
Tadini, G1
Barbareschi, M1
Menni, S1
Caputo, R1
Nichols, DD1
Bottini, AG1
Martínez-Frías, ML1
Arroyo Carrera, I1
Muñoz-Delgado, NJ1
Nieto Conde, C1
Rodríguez-Pinilla, E1
Urioste Azcorra, M1
Omeñaca Teres, F1
García Alix, A1
Elliott, AM1
Teebi, AS1
Mastruserio, DN1
Cobb, MA1
Ross, VE1
Kruk-Jeromin, J1
Janik, J1
Rykała, J1
Madsen, JR1
Robertson, RL1
Bartlett, R1
Rasheed, T1
Orlando, A1
Gordon, DJ1
Uppal, RS1
Moss, AL1
Gündüz, K1
Shields, CL1
Doych, Y1
Schnall, B1
Shields, JA1
Yang, JY1
Yang, WG1
Koshy, CE1
Waterhouse, N1
Peterson, D1
Islamoglu, K1
Ozgentas, E1
Casanova, D1
Amar, E1
Bardot, J1
Magalon, G1
Atasua, M1
Dumlu, A1
Ozbayrak, S1
Vinocur, CD1
Weintraub, WH1
Wilensky, RJ1
Coran, AG1
Dingman, RO1
Barnett, AB1
Ott, R1
Laub, DR1
Demmel, U1
Scribanu, N1
Temtamy, SA1
Solomon, LM1
Bork, K1
Pfeifle, J1
Attalla, MF1
el-Sayed, AM1
Blunt, K1
Quan, V1
Carr, D1
Paes, BA1
Stratis, JP1
Ramer, JC1
Manders, EK1
Lehman, RA1
Ladda, RL1
Gücüyener, K1
Tunaoglu, FS1
Demirsoy, S1
Atalay, Y1
Memioglu, N1
Dallapiccola, B1
Giannotti, A1
Marino, B1
Digilio, C1
Obregon, G1
Moscona, R1
Berger, J1
Govrin, J1
Breslau-Siderius, EJ1
Lavrijsen, AP1
Otten, FW1
van der Schroeff, JG1
Swart, JG1
Paltzik, RL1
Aiello, AM1
Muller, SA1
Croce, EJ1
Purohit, RC1
Janovski, NA1
Bianchine, JW1
Mahrle, G1
Salamon, T1
Vissian, L1
Martin, J1
Vaillaud, JC1
Maissa, S1
Pap, GS1
Pear, BL1
Deeken, JH1
Caplan, RM1

Reviews

14 reviews available for salicylic acid and Anhidrotic Ectodermal Dysplasia

ArticleYear
Aplasia cutis congenita in Korea: Single center experience and literature review.
    Pediatrics international : official journal of the Japan Pediatric Society, 2020, Volume: 62, Issue:7

    Topics: Administration, Topical; Adolescent; Child; Child, Preschool; Ectodermal Dysplasia; Female; Humans;

2020
Scalp-Ear-Nipple syndrome: first report of a Potassium channel tetramerization domain-containing 1 in-frame insertion and review of the literature.
    Clinical dysmorphology, 2021, Oct-01, Volume: 30, Issue:4

    Topics: Abnormalities, Multiple; Child; Co-Repressor Proteins; Ear, External; Ectodermal Dysplasia; Humans;

2021
Aplasia cutis congenita type V: a case report and review of the literature.
    International journal of dermatology, 2017, Volume: 56, Issue:6

    Topics: Anti-Infective Agents, Local; Ectodermal Dysplasia; Humans; Infant; Male; Prognosis; Scalp; Silver S

2017
Fatal superior sagittal sinus hemorrhage as a complication of aplasia cutis congenita: a case report and literature review.
    Forensic science, medicine, and pathology, 2015, Volume: 11, Issue:2

    Topics: Ectodermal Dysplasia; Fatal Outcome; Female; Hemorrhage; Humans; Infant, Newborn; Scalp; Skull; Subc

2015
Aplasia Cutis Congenita of the Scalp, Composite Type: The Criticality and Inseparability of Neurosurgical and Plastic Surgical Management.
    Pediatric neurosurgery, 2016, Volume: 51, Issue:3

    Topics: Disease Management; Ectodermal Dysplasia; Female; Humans; Infant; Infant, Newborn; Male; Plastic Sur

2016
Systemic aplasia cutis congenita: A case report and review of the literature.
    Pathology, research and practice, 2010, Jul-15, Volume: 206, Issue:7

    Topics: Abnormalities, Multiple; Ectodermal Dysplasia; Female; Humans; Infant, Newborn; Scalp; Skin; Skull

2010
Aplasia cutis congenita of the scalp, the skull, and the dura.
    Scandinavian journal of plastic and reconstructive surgery and hand surgery, 2003, Volume: 37, Issue:3

    Topics: Dura Mater; Ectodermal Dysplasia; Humans; Infant, Newborn; Male; Scalp; Skull; Surgical Flaps

2003
Aplasia cutis congenita of the scalp: is there a better treatment strategy?
    Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2006, Volume: 22, Issue:9

    Topics: Abnormalities, Multiple; Bone Transplantation; Child, Preschool; Diseases in Twins; Ectodermal Dyspl

2006
Aplasia cutis congenita of the scalp. Report of 16 cases.
    Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.], 1998, Volume: 24, Issue:5

    Topics: Adolescent; Child; Child, Preschool; Ectodermal Dysplasia; Female; Humans; Male; Scalp; Surgical Fla

1998
Ocular ectodermal syndrome of epibulbar dermoid and cutaneous myxovascular hamartoma.
    The British journal of ophthalmology, 2000, Volume: 84, Issue:6

    Topics: Dermoid Cyst; Ectodermal Dysplasia; Eye Neoplasms; Hemangioma; Humans; Infant, Newborn; Male; Scalp;

2000
A case of Adams-Oliver syndrome associated with acrania, microcephaly, hemiplegia, epilepsy, and mental retardation.
    Acta neurologica Belgica, 2000, Volume: 100, Issue:4

    Topics: Abnormalities, Multiple; Consanguinity; Ectodermal Dysplasia; Epilepsy, Tonic-Clonic; Fingers; Growt

2000
Clinical aspects of congenital skin defects. I. Congenital skin defects on the head of the newborn.
    European journal of pediatrics, 1975, Dec-09, Volume: 121, Issue:1

    Topics: Abnormalities, Multiple; Amnion; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Dis

1975
Aplasia cutis congenita: a clinical review and associated defects.
    Neonatal network : NN, 1992, Volume: 11, Issue:7

    Topics: Ectodermal Dysplasia; Education, Nursing, Continuing; Female; Humans; Infant, Newborn; Neonatal Nurs

1992
Alopecia: syndromes of genetic significance.
    The Journal of investigative dermatology, 1973, Volume: 60, Issue:6

    Topics: Abnormalities, Multiple; Adolescent; Adult; Age Factors; Alopecia; Alopecia Areata; Child; Child, Pr

1973

Other Studies

167 other studies available for salicylic acid and Anhidrotic Ectodermal Dysplasia

ArticleYear
[An infant with multiple lesions of the scalp].
    Nederlands tijdschrift voor geneeskunde, 2021, 08-18, Volume: 165

    Topics: Ectodermal Dysplasia; Humans; Infant; Male; Scalp; Skin Diseases

2021
A novel DLL4 mutation in Adams-Oliver syndrome with absence of the right pulmonary artery in newborn.
    American journal of medical genetics. Part A, 2022, Volume: 188, Issue:2

    Topics: Adaptor Proteins, Signal Transducing; Calcium-Binding Proteins; Ectodermal Dysplasia; Humans; Infant

2022
Challenges in the management of extensive aplasia cutis congenita.
    BMJ case reports, 2022, Feb-14, Volume: 15, Issue:2

    Topics: Bandages; Child; Ectodermal Dysplasia; Female; Hemorrhage; Humans; Infant; Scalp; Skin

2022
Trichorhinophalangeal syndrome type II associated with aplasia cutis congenita in a neonate.
    Pediatric dermatology, 2022, Volume: 39, Issue:3

    Topics: Ectodermal Dysplasia; Humans; Infant, Newborn; Langer-Giedion Syndrome; Limb Deformities, Congenital

2022
Severe Adams-Oliver Syndrome after Maternal COVID-19 Infection Could Be Another Effect of the SARS-CoV-2 Inflammatory Storm? Case Report.
    Fetal and pediatric pathology, 2023, Volume: 42, Issue:1

    Topics: COVID-19; Ectodermal Dysplasia; Humans; Limb Deformities, Congenital; SARS-CoV-2; Scalp

2023
Maternal SARS-CoV-2 infection and aplasia cutis congenita in a newborn.
    Journal of the European Academy of Dermatology and Venereology : JEADV, 2022, Volume: 36, Issue:11

    Topics: COVID-19; Ectodermal Dysplasia; Humans; Infant, Newborn; SARS-CoV-2; Scalp

2022
[A child with a bald spot on her scalp].
    Nederlands tijdschrift voor geneeskunde, 2022, 07-18, Volume: 166

    Topics: Alopecia; Ectodermal Dysplasia; Family; Female; Humans; Infant; Rare Diseases; Scalp

2022
A Drosophila Su(H) model of Adams-Oliver Syndrome reveals cofactor titration as a mechanism underlying developmental defects.
    PLoS genetics, 2022, Volume: 18, Issue:8

    Topics: Animals; Co-Repressor Proteins; DNA; Drosophila; Drosophila Proteins; Ectodermal Dysplasia; Humans;

2022
Dermoscopic characteristics of membranous aplasia cutis congenita: Report of 56 cases.
    Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI), 2022, Volume: 28, Issue:6

    Topics: Ectodermal Dysplasia; Epidermis; Hair; Hair Follicle; Humans; Infant; Infant, Newborn; Scalp

2022
Cutaneous squamous cell carcinoma in an autosomal-recessive Adams-Oliver syndrome patient with a novel frameshift pathogenic variant in the EOGT gene.
    American journal of medical genetics. Part A, 2022, Volume: 188, Issue:11

    Topics: Carcinoma, Squamous Cell; Ectodermal Dysplasia; Female; Frameshift Mutation; Humans; Limb Deformitie

2022
FOSL2 truncating variants in the last exon cause a neurodevelopmental disorder with scalp and enamel defects.
    Genetics in medicine : official journal of the American College of Medical Genetics, 2022, Volume: 24, Issue:12

    Topics: Autism Spectrum Disorder; Ectodermal Dysplasia; Exons; Fos-Related Antigen-2; HEK293 Cells; Humans;

2022
Intrafamilial phenotypic variability in autosomal recessive DOCK6-related Adams-Oliver syndrome.
    European journal of medical genetics, 2022, Volume: 65, Issue:12

    Topics: Biological Variation, Population; Ectodermal Dysplasia; Female; Guanine Nucleotide Exchange Factors;

2022
Case Report: Anesthesia for a Neonate With Cutis Aplasia.
    A&A practice, 2022, Oct-01, Volume: 16, Issue:10

    Topics: Anesthesia; Ectodermal Dysplasia; Female; Humans; Infant, Newborn; Scalp

2022
Triple Dufourmentel hexagonal flap for scalp reconstruction.
    Experimental dermatology, 2023, Volume: 32, Issue:5

    Topics: Ectodermal Dysplasia; Humans; Plastic Surgery Procedures; Scalp; Surgical Flaps

2023
Homozygosity for a novel DOCK6 variant in an individual without aplasia cutis congenita of the scalp and terminal transverse limb defects.
    Clinical dysmorphology, 2023, 04-01, Volume: 32, Issue:2

    Topics: Abnormalities, Multiple; Ectodermal Dysplasia; Guanine Nucleotide Exchange Factors; Humans; Limb Def

2023
Trichoscopy of aplasia cutis congenita of the scalp in skin of color.
    Journal of cosmetic dermatology, 2023, Volume: 22, Issue:7

    Topics: Ectodermal Dysplasia; Humans; Scalp; Skin; Skin Pigmentation

2023
A rare case of extensive aplasia cutis congenita: Our surgical approach.
    Journal of plastic, reconstructive & aesthetic surgery : JPRAS, 2023, Volume: 80

    Topics: Ectodermal Dysplasia; Humans; Scalp; Skin; Skin Transplantation; Surgical Flaps

2023
Aplasia Cutis Congenita of the Scalp with Bone Defect and Exposed Sagittal Sinus in Trisomy 13 Newborn - a Case Report.
    Medical archives (Sarajevo, Bosnia and Herzegovina), 2023, Volume: 77, Issue:4

    Topics: Brain; Ectodermal Dysplasia; Female; Humans; Infant, Newborn; Scalp; Skull; Trisomy 13 Syndrome

2023
Aplasia cutis congenita of the scalp: Histopathologic features and clinicopathologic correlation in a case series.
    Journal of cutaneous pathology, 2020, Volume: 47, Issue:5

    Topics: Adolescent; Adult; Child; Child, Preschool; Cicatrix; Ectodermal Dysplasia; Elastic Tissue; Female;

2020
Low risk of clinically important central nervous system dysraphism in a cohort study of 69 patients with isolated aplasia cutis congenita of the head.
    Pediatric dermatology, 2020, Volume: 37, Issue:3

    Topics: Child; Cohort Studies; Ectodermal Dysplasia; Humans; Retrospective Studies; Scalp; Skull

2020
Bullous aplasia cutis congenita: A rare presentation of a rare disease.
    Dermatology online journal, 2020, Feb-15, Volume: 26, Issue:2

    Topics: Ectodermal Dysplasia; Female; Humans; Infant, Newborn; Rare Diseases; Scalp; Scalp Dermatoses

2020
Multiple Aplasia Cutis Congenita Lesions of the Scalp: A Case Study.
    Neonatal network : NN, 2020, Mar-01, Volume: 39, Issue:2

    Topics: Chromosome Aberrations; Ectodermal Dysplasia; Female; Genetic Predisposition to Disease; Humans; Inf

2020
Classification of aplasia cutis congenita: a 25-year review of cases presenting to a tertiary paediatric dermatology department.
    Clinical and experimental dermatology, 2020, Volume: 45, Issue:8

    Topics: Abnormalities, Multiple; Child; Child, Preschool; Cleft Palate; Dermatology; Ectodermal Dysplasia; E

2020
Adams-Oliver syndrome: a case of bilateral progressive ischemic maculopathy.
    Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus, 2020, Volume: 24, Issue:3

    Topics: Ectodermal Dysplasia; Female; Humans; Infant; Limb Deformities, Congenital; Macular Degeneration; Ma

2020
Type V aplasia cutis congenita in a preterm newborn successfully resolved.
    Dermatologic therapy, 2020, Volume: 33, Issue:6

    Topics: Bandages; Ectodermal Dysplasia; Humans; Infant, Newborn; Male; Petrolatum; Scalp; Torso

2020
Pseudo-cobra neck deformity due to aplasia cutis congenita.
    International journal of pediatric otorhinolaryngology, 2020, Volume: 139

    Topics: Ectodermal Dysplasia; Humans; Scalp; Skin

2020
Aplasia cutis congenita in a CDC42-related developmental phenotype.
    American journal of medical genetics. Part A, 2021, Volume: 185, Issue:3

    Topics: Abnormalities, Multiple; Adult; Amino Acid Substitution; cdc42 GTP-Binding Protein; Craniofacial Abn

2021
Multidisciplinary management of a previously unreported presentation of severe aplasia cutis congenita.
    Pediatric dermatology, 2021, Volume: 38, Issue:2

    Topics: Ectodermal Dysplasia; Humans; Infant; Infant, Newborn; Male; Scalp; Skin

2021
Aplasia cutis congenita with dermal melanocytosis.
    The Australasian journal of dermatology, 2021, Volume: 62, Issue:2

    Topics: Alopecia; Child; Ectodermal Dysplasia; Female; Genetic Diseases, X-Linked; Humans; Scalp

2021
Frieden's type 7 aplasia cutis congenita in a premature neonate.
    Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG, 2021, Volume: 19, Issue:5

    Topics: Ectodermal Dysplasia; Female; Humans; Infant, Newborn; Pregnancy; Pregnancy Complications; Scalp

2021
Temporal triangular alopecia confined to the frontal scalp.
    The Journal of dermatology, 2021, Volume: 48, Issue:4

    Topics: Alopecia; Ectodermal Dysplasia; Hair; Humans; Scalp; Skin

2021
A Case of Large Aplasia Cutis Congenita with Underlying Skull Defect: Effective Surgical Treatment with Integra® Dermal Regeneration Template.
    Pediatric neurosurgery, 2021, Volume: 56, Issue:3

    Topics: Ectodermal Dysplasia; Humans; Infant, Newborn; Scalp; Skin Transplantation; Skull; Surgical Flaps

2021
Aplasia Cutis Congenita: A Case Report.
    West African journal of medicine, 2021, Apr-23, Volume: 38, Issue:4

    Topics: Ectodermal Dysplasia; Humans; Infant, Newborn; Scalp; Skin; Skull

2021
APLASIA CUTIS CONGENITA TYPE I - A CASE SERIES.
    Georgian medical news, 2017, Issue:264

    Topics: Ectodermal Dysplasia; Extremities; Female; Humans; Infant; Male; Scalp

2017
Use of an epidermal growth factor-infused foam dressing in a complicated case of Adams-Oliver syndrome.
    Journal of wound care, 2017, 06-02, Volume: 26, Issue:6

    Topics: Bandages; Child, Preschool; Ectodermal Dysplasia; Epidermal Growth Factor; Humans; Imaging, Three-Di

2017
Multiple-opposing rotation flaps for the scalp defect including hair whorl.
    The Journal of dermatology, 2017, Volume: 44, Issue:11

    Topics: Carcinoma, Basal Cell; Ectodermal Dysplasia; Humans; Plastic Surgery Procedures; Scalp; Scalp Dermat

2017
Erosive pustular dermatosis of the scalp after aplasia cutis congenita in a 9-year-old patient: A 5-year follow-up.
    Pediatric dermatology, 2017, Volume: 34, Issue:6

    Topics: Child; Ectodermal Dysplasia; Female; Follow-Up Studies; Glucocorticoids; Humans; Scalp; Scalp Dermat

2017
Clinical Application of Acellular Dermal Matrix in the Treatment of Aplasia Cutis Congenita on Scalp.
    The Journal of craniofacial surgery, 2017, Volume: 28, Issue:8

    Topics: Acellular Dermis; Conservative Treatment; Ectodermal Dysplasia; Humans; Infant, Newborn; Male; Scalp

2017
Congenital Absence of Skin on Scalp.
    The Journal of pediatrics, 2018, Volume: 196

    Topics: Conservative Treatment; Ectodermal Dysplasia; Humans; Infant, Newborn; Male; Scalp; Skin

2018
Erythematous Lesion on a Newborn's Scalp.
    American family physician, 2017, Nov-15, Volume: 96, Issue:10

    Topics: Diagnosis, Differential; Ectodermal Dysplasia; Erythema; Female; Humans; Infant, Newborn; Scalp

2017
Elucidating the genetic architecture of Adams-Oliver syndrome in a large European cohort.
    Human mutation, 2018, Volume: 39, Issue:9

    Topics: Ectodermal Dysplasia; Extremities; Female; Genetic Association Studies; Humans; Limb Deformities, Co

2018
Pseudodidymosis: nevus psiloliparus with aplasia cutis congenita, an initial manifestation of Haberland syndrome.
    International journal of dermatology, 2018, Volume: 57, Issue:12

    Topics: Adipose Tissue; Alopecia; Child; Ectodermal Dysplasia; Eye Diseases; Genetic Pleiotropy; Humans; Lip

2018
Wooly hair nevus, Post's Type 2.
    International journal of dermatology, 2019, Volume: 58, Issue:10

    Topics: Child, Preschool; Diagnosis, Differential; Ectodermal Dysplasia; Facies; Failure to Thrive; Female;

2019
Extensive aplasia cutis congenita associated with cephalocranial disproportion and brain extrusion.
    Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2019, Volume: 35, Issue:9

    Topics: Craniosynostoses; Craniotomy; Decompression, Surgical; Dura Mater; Ectodermal Dysplasia; Female; Hum

2019
Two cases of aplasia cutis congenita with hair collar signs and macrophage hyperplasia.
    The Journal of dermatology, 2019, Volume: 46, Issue:8

    Topics: Dermoscopy; Ectodermal Dysplasia; Female; Hair Follicle; Hemangioma; Humans; Infant; Macrophages; Me

2019
Mercedes Flap With Modified "V-Y" Releasing Incisions for Scalp Defects.
    Annals of plastic surgery, 2020, Volume: 84, Issue:2

    Topics: Ectodermal Dysplasia; Humans; Plastic Surgery Procedures; Scalp; Surgical Flaps

2020
Aplasia cutis congenita of the scalp in a female infant with anophthalmia/microphthalmia-esophageal atresia syndrome negative for SOX2 mutation.
    American journal of medical genetics. Part A, 2013, Volume: 161A, Issue:5

    Topics: Ectodermal Dysplasia; Esophageal Atresia; Female; Humans; Infant; Microphthalmos; Mutation; Nervous

2013
Aplasia cutis congenita--a case study of a family with two siblings with this disorder.
    South Dakota medicine : the journal of the South Dakota State Medical Association, 2013, Volume: 66, Issue:2

    Topics: Ectodermal Dysplasia; Family; Female; Humans; Infant, Newborn; Scalp; Siblings; Skin

2013
Mutations in KCTD1 cause scalp-ear-nipple syndrome.
    American journal of human genetics, 2013, Apr-04, Volume: 92, Issue:4

    Topics: Abnormalities, Multiple; Amino Acid Sequence; Branchio-Oto-Renal Syndrome; Co-Repressor Proteins; Ea

2013
A rare case of aplasia cutis congenita.
    Acta medica Iranica, 2013, May-30, Volume: 51, Issue:5

    Topics: Diagnosis, Differential; Ectodermal Dysplasia; Female; Humans; Infant, Newborn; Scalp; Skin

2013
BMS1 is mutated in aplasia cutis congenita.
    PLoS genetics, 2013, Volume: 9, Issue:6

    Topics: Cell Proliferation; Chromosome Mapping; Ectodermal Dysplasia; Female; Genetic Linkage; Genome, Human

2013
Aplasia cutis congenital: a case of large scalp and skull defects treated with conservative approach.
    Chinese medical journal, 2013, Volume: 126, Issue:14

    Topics: Ectodermal Dysplasia; Humans; Infant; Male; Scalp; Skull

2013
Adams-Oliver syndrome.
    International journal of dermatology, 2014, Volume: 53, Issue:3

    Topics: Bandages; Ectodermal Dysplasia; Female; Genes, Dominant; Humans; Infant, Newborn; Limb Deformities,

2014
Epidermal nevus in association with some uncommon manifestations.
    Acta dermatovenerologica Croatica : ADC, 2013, Volume: 21, Issue:4

    Topics: Consanguinity; DNA Mutational Analysis; Ectodermal Dysplasia; Female; Fractures, Bone; Head and Neck

2013
Isolated terminal limb reduction defects: extending the clinical spectrum of Adams-Oliver syndrome and ARHGAP31 mutations.
    American journal of medical genetics. Part A, 2014, Volume: 164A, Issue:6

    Topics: Ectodermal Dysplasia; Family; Female; GTPase-Activating Proteins; Humans; Immunoglobulin J Recombina

2014
Adams-Oliver syndrome.
    Journal of the College of Physicians and Surgeons--Pakistan : JCPSP, 2014, Volume: 24 Suppl 2

    Topics: Abnormalities, Multiple; Ectodermal Dysplasia; Foot Deformities, Congenital; Humans; Infant; Limb De

2014
Aplasia cutis with 'hair collar sign'.
    Archives of disease in childhood, 2014, Volume: 99, Issue:11

    Topics: Ectodermal Dysplasia; Hair; Humans; Infant; Male; Scalp

2014
Aplasia cutis congenita: clinical management and a new classification system.
    Plastic and reconstructive surgery, 2014, Volume: 134, Issue:5

    Topics: Ectodermal Dysplasia; Female; Follow-Up Studies; Graft Rejection; Graft Survival; Heel; Humans; Infa

2014
Aplasia cutis congenita presenting as vacuum-extractor-related trauma.
    International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics, 2015, Volume: 129, Issue:3

    Topics: Birth Injuries; Cesarean Section; Diagnosis, Differential; Ectodermal Dysplasia; Humans; Infant, New

2015
[Surgical management of aplasia cutis congenita].
    Anales de pediatria (Barcelona, Spain : 2003), 2015, Volume: 83, Issue:5

    Topics: Child; Ectodermal Dysplasia; Humans; Retrospective Studies; Scalp; Skin Transplantation; Surgical Fl

2015
Oculoectodermal syndrome is a mosaic RASopathy associated with KRAS alterations.
    American journal of medical genetics. Part A, 2015, Volume: 167, Issue:7

    Topics: Base Sequence; Child; Child, Preschool; Choristoma; Corneal Diseases; Dermoid Cyst; Ectodermal Dyspl

2015
[Circumscribed aplasia cutis congenita of the scalp in a Rwandan child: about an observation].
    The Pan African medical journal, 2014, Volume: 19

    Topics: Ectodermal Dysplasia; Female; Humans; Infant, Newborn; Magnetic Resonance Imaging; Prognosis; Rwanda

2014
Successful conservative management of a large congenital scalp and skull defect.
    The Journal of craniofacial surgery, 2015, Volume: 26, Issue:3

    Topics: Bandages; Cesarean Section; Ectodermal Dysplasia; Female; Humans; Infant; Infant, Newborn; Pregnancy

2015
Our experience with a severe case of aplasia cutis congenita with a large skull defect.
    International journal of dermatology, 2016, Volume: 55, Issue:10

    Topics: Abnormalities, Multiple; Anti-Bacterial Agents; Chromosome Disorders; Chromosomes, Human, Pair 13; D

2016
Adams Oliver Syndrome.
    Indian pediatrics, 2015, Volume: 52, Issue:7

    Topics: Ectodermal Dysplasia; Female; Humans; Infant; Limb Deformities, Congenital; Scalp; Scalp Dermatoses;

2015
Calvarial Regeneration With Use of Acellular Dermal Matrix in Aplasia Cutis Congenita.
    The Journal of craniofacial surgery, 2015, Volume: 26, Issue:6

    Topics: Acellular Dermis; Bone Regeneration; Cranial Sinuses; Dura Mater; Ectodermal Dysplasia; Follow-Up St

2015
Outcomes of Tissue Expander Application for Scalp Reconstruction in Extensive Aplasia Cutis Congenita.
    Aesthetic plastic surgery, 2016, Volume: 40, Issue:1

    Topics: Adult; Child; Child, Preschool; Ectodermal Dysplasia; Female; Humans; Male; Plastic Surgery Procedur

2016
Technique for Management of Aplasia Cutis Congenita of the Scalp With a Skin Allograft.
    The Journal of craniofacial surgery, 2016, Volume: 27, Issue:4

    Topics: Allografts; Ectodermal Dysplasia; Female; Humans; Infant, Newborn; Plastic Surgery Procedures; Scalp

2016
A Novel Local Autologous Bone Graft Donor Site After Scalp Tissue Expansion in Aplasia Cutis Congenita.
    The Journal of craniofacial surgery, 2016, Volume: 27, Issue:4

    Topics: Bone Transplantation; Child, Preschool; Ectodermal Dysplasia; Female; Follow-Up Studies; Humans; Inf

2016
Bullous Kaposiform Hemangioendothelioma Masquerading as Aplasia Cutis Congenita.
    Pediatric dermatology, 2016, Volume: 33, Issue:5

    Topics: Diagnosis, Differential; Ectodermal Dysplasia; Hemangioendothelioma; Humans; Infant; Kasabach-Merrit

2016
Expression studies of nectin-1 in human hair follicles and identification of a p63-responsive element in the NECTIN1 promoter.
    Journal of dermatological science, 2016, Volume: 84, Issue:2

    Topics: Adherens Junctions; Cell Adhesion Molecules; Ectodermal Dysplasia; Epidermis; Fluorescent Antibody T

2016
[Aplasia cutis congenita].
    Handchirurgie, Mikrochirurgie, plastische Chirurgie : Organ der Deutschsprachigen Arbeitsgemeinschaft fur Handchirurgie : Organ der Deutschsprachigen Arbeitsgemeinschaft fur Mikrochirurgie der Peripheren Nerven und Gefasse : Organ der V..., 2016, Volume: 48, Issue:4

    Topics: Bandages; Ectodermal Dysplasia; Humans; Infant, Newborn; Scalp; Skin

2016
Aplasia cutis congenita and amniotic band syndrome: an uncommon association.
    BMJ case reports, 2017, Jan-31, Volume: 2017

    Topics: Amniotic Band Syndrome; Ectodermal Dysplasia; Female; Humans; Infant, Newborn; Scalp

2017
Aplasia cutis congenita of the scalp, skull and dura associated with Adams-Oliver syndrome.
    Turkish neurosurgery, 2008, Volume: 18, Issue:2

    Topics: Abnormalities, Multiple; Brain; Dura Mater; Ectodermal Dysplasia; Fatal Outcome; Humans; Infant, New

2008
Aplasia cutis congenita of the scalp.
    Arquivos de neuro-psiquiatria, 2008, Volume: 66, Issue:3B

    Topics: Ectodermal Dysplasia; Female; Humans; Infant, Newborn; Scalp

2008
Rationale and background as basis for a new classification of the ectodermal dysplasias.
    American journal of medical genetics. Part A, 2009, Volume: 149A, Issue:9

    Topics: Child, Preschool; Ectodermal Dysplasia; Genotype; Hair; Humans; Male; Molecular Biology; Nails; Phen

2009
Aplasia cutis congenita. A case of scalp defect repair using two opposing bipedicled local flaps.
    Journal of plastic, reconstructive & aesthetic surgery : JPRAS, 2010, Volume: 63, Issue:3

    Topics: Ectodermal Dysplasia; Female; Humans; Infant, Newborn; Scalp; Surgical Flaps

2010
Aplasia cutis congenita: management of a large skull defect with acrania.
    The Journal of craniofacial surgery, 2009, Volume: 20, Issue:4

    Topics: Dura Mater; Ectodermal Dysplasia; Female; Humans; Infant, Newborn; Scalp; Skull; Tomography, X-Ray C

2009
Clinical lessons learned from the International Research Symposium on Ankyloblepharon-Ectodermal Defects-Cleft Lip/Palate (AEC) syndrome.
    American journal of medical genetics. Part A, 2009, Volume: 149A, Issue:9

    Topics: Abnormalities, Multiple; Adolescent; Adult; Child; Child, Preschool; Cleft Lip; Cleft Palate; Ectode

2009
Dermatologic findings of ankyloblepharon-ectodermal defects-cleft lip/palate (AEC) syndrome.
    American journal of medical genetics. Part A, 2009, Volume: 149A, Issue:9

    Topics: Abnormalities, Multiple; Adolescent; Adult; Child; Child, Preschool; Cleft Lip; Cleft Palate; Ectode

2009
Management of large scalp and skull defects in a severe case of Adams-Oliver syndrome.
    Journal of neurosurgery. Pediatrics, 2009, Volume: 4, Issue:6

    Topics: Abnormalities, Multiple; Bandages; Dura Mater; Ectodermal Dysplasia; Female; Hand Deformities, Conge

2009
[The Adams-Oliver syndrome. A case report].
    Chirurgie de la main, 2010, Volume: 29, Issue:4

    Topics: Abnormalities, Multiple; Alopecia; Ectodermal Dysplasia; Female; Finger Phalanges; Foot Deformities,

2010
[Adams-Oliver syndrome: a case with minimal expression].
    Archives de pediatrie : organe officiel de la Societe francaise de pediatrie, 2010, Volume: 17, Issue:10

    Topics: Ectodermal Dysplasia; Fingers; Foot Deformities, Congenital; Hand Deformities, Congenital; Humans; I

2010
Herniation of the brain after conservative treatment of a large congenital skull defect in an infant with Adams-Oliver syndrome.
    Journal of pediatric surgery, 2010, Volume: 45, Issue:10

    Topics: Cerebrospinal Fluid Leak; Cerebrospinal Fluid Rhinorrhea; Cerebrospinal Fluid Shunts; Ectodermal Dys

2010
Aplasia cutis congenita of the scalp.
    Turkish neurosurgery, 2010, Volume: 20, Issue:4

    Topics: Ectodermal Dysplasia; Humans; Infant, Newborn; Scalp; Skin Transplantation

2010
Aplasia cutis congenita: clinical management of a rare congenital anomaly.
    The Journal of craniofacial surgery, 2011, Volume: 22, Issue:1

    Topics: Bandages; Ectodermal Dysplasia; Female; Humans; Infant, Newborn; Magnetic Resonance Imaging; Plastic

2011
Anophthalmia in fronto-facial-nasal dysplasia.
    Clinical dysmorphology, 2011, Volume: 20, Issue:2

    Topics: Abnormalities, Multiple; Adolescent; Anophthalmos; Autistic Disorder; Cleft Lip; Cleft Palate; Crani

2011
Aplasia cutis congenita with hair collar sign and dermal melanocytosis.
    International journal of dermatology, 2012, Volume: 51, Issue:6

    Topics: Dermis; Ectodermal Dysplasia; Female; Humans; Infant; Melanocytes; Scalp

2012
Aplasia cutis congenita of the trunk and scalp associated with fetus papyraceus.
    International journal of dermatology, 2011, Volume: 50, Issue:6

    Topics: Abdominal Wall; Adult; Diseases in Twins; Ectodermal Dysplasia; Female; Fetal Diseases; Humans; Infa

2011
Autosomal dominant aplasia cutis in three generations and one case with preaxial polydactyly in the last generation.
    Genetic counseling (Geneva, Switzerland), 2011, Volume: 22, Issue:1

    Topics: Chromosome Aberrations; Ectodermal Dysplasia; Female; Genes, Dominant; Humans; Infant; Infant, Newbo

2011
Reconstruction of complex aplasia cutis congenita.
    The Journal of craniofacial surgery, 2012, Volume: 23, Issue:2

    Topics: Ectodermal Dysplasia; Humans; Infant, Newborn; Plastic Surgery Procedures; Scalp; Skull

2012
Management of aplasia cutis congenita of the scalp.
    The Journal of craniofacial surgery, 2012, Volume: 23, Issue:6

    Topics: Ectodermal Dysplasia; Female; Humans; Infant; Infant, Newborn; Male; Postoperative Complications; Re

2012
Dilemmas and challenges in the management of a neonate with Adams-Oliver syndrome with infected giant aplasia cutis lesion and exsanguination: a case-based update.
    Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2013, Volume: 29, Issue:4

    Topics: Debridement; Ectodermal Dysplasia; Exsanguination; Female; Humans; Infant; Limb Deformities, Congeni

2013
Scalp erosion in ankyloblepharon-ectodermal defect-cleft lip and/or palate (AEC syndrome): treatment with acellular dermal matrix.
    The Journal of craniofacial surgery, 2013, Volume: 24, Issue:1

    Topics: Anti-Bacterial Agents; Bandages; Chondroitin Sulfates; Cleft Lip; Cleft Palate; Collagen; Debridemen

2013
Our experience with aplasia cutis congenita.
    The Journal of dermatology, 2002, Volume: 29, Issue:6

    Topics: Ectodermal Dysplasia; Fatal Outcome; Female; Humans; Infant, Newborn; Male; Scalp

2002
Complete osseous regeneration of a large skull defect in a patient with cutis aplasia: a conservative approach.
    The Journal of craniofacial surgery, 2002, Volume: 13, Issue:4

    Topics: Administration, Cutaneous; Administration, Oral; Alopecia; Anti-Infective Agents; Anti-Infective Age

2002
Surgical treatment of aplasia cutis congenita of the scalp associated with bilateral coronal synostosis.
    The Journal of craniofacial surgery, 2002, Volume: 13, Issue:4

    Topics: Alopecia; Bone Transplantation; Cicatrix; Craniosynostoses; Ectodermal Dysplasia; Follow-Up Studies;

2002
[Congenital cutaneous aplasia of the scalp vertex in a newborn].
    Archives de pediatrie : organe officiel de la Societe francaise de pediatrie, 2002, Volume: 9, Issue:9

    Topics: Adult; Ectodermal Dysplasia; Female; Humans; Infant, Newborn; Patient Care Team; Pregnancy; Prognosi

2002
[Aplasia cutis congenita in 4 infants].
    Nederlands tijdschrift voor geneeskunde, 2002, Nov-23, Volume: 146, Issue:47

    Topics: Ectodermal Dysplasia; Humans; Scalp; Skin Transplantation

2002
Management of aplasia cutis congenita of the scalp: a continuing enigma.
    British journal of plastic surgery, 2002, Volume: 55, Issue:8

    Topics: Biological Dressings; Ectodermal Dysplasia; Follow-Up Studies; Humans; Infant, Newborn; Male; Scalp

2002
Aplasia cutis cerebri with partial acrania--total reconstruction in a severe case and review of the literature.
    Journal of pediatric surgery, 2003, Volume: 38, Issue:2

    Topics: Dura Mater; Ectodermal Dysplasia; Female; Humans; Infant, Newborn; Parietal Bone; Radiography; Scalp

2003
[Rapp-Hodgkin's syndrome: two cases].
    Annales de dermatologie et de venereologie, 2003, Volume: 130, Issue:3

    Topics: Adult; Child, Preschool; Craniofacial Abnormalities; Dermatitis; Ectodermal Dysplasia; Humans; Hypoh

2003
Congenital scalp defect.
    New York state journal of medicine, 1954, Mar-15, Volume: 54, Issue:6

    Topics: Congenital Abnormalities; Ectodermal Dysplasia; Head; Humans; Limb Deformities, Congenital; Scalp; S

1954
Congenital absence of the scalp and skull.
    Annals of surgery, 1956, Volume: 144, Issue:6

    Topics: Ectodermal Dysplasia; Head; Humans; Medical Records; Scalp; Skull

1956
Congenital absence of the scalp and skull.
    Annals of surgery, 1956, Volume: 144, Issue:6

    Topics: Ectodermal Dysplasia; Head; Humans; Medical Records; Scalp; Skull

1956
Congenital absence of the scalp and skull.
    Annals of surgery, 1956, Volume: 144, Issue:6

    Topics: Ectodermal Dysplasia; Head; Humans; Medical Records; Scalp; Skull

1956
Congenital absence of the scalp and skull.
    Annals of surgery, 1956, Volume: 144, Issue:6

    Topics: Ectodermal Dysplasia; Head; Humans; Medical Records; Scalp; Skull

1956
Congenital absence of skin (aplasia cutis congenita).
    Plastic and reconstructive surgery and the transplantation bulletin, 1960, Volume: 26

    Topics: Ectodermal Dysplasia; Humans; Scalp; Skin; Skin Abnormalities

1960
CONGENITAL SCALP DEFECTS IN TWIN SISTERS.
    American journal of diseases of children (1960), 1965, Volume: 110

    Topics: Congenital Abnormalities; Diseases in Twins; Ectodermal Dysplasia; Female; Humans; Infant; Infant, N

1965
CONGENITAL SCALP DEFECTS IN FATHER AND SON.
    American journal of diseases of children (1960), 1965, Volume: 110

    Topics: Congenital Abnormalities; Ectodermal Dysplasia; Fathers; Genetics, Medical; Humans; Infant; Infant,

1965
Malformations following methimazole exposure in utero: an open issue.
    Birth defects research. Part A, Clinical and molecular teratology, 2003, Volume: 67, Issue:12

    Topics: Abnormalities, Drug-Induced; Antithyroid Agents; Ectodermal Dysplasia; Female; Humans; Hyperthyroidi

2003
Aplasia cutis congenita, polythelia, microcephaly, and developmental delay: a unique expression of polytopic field defect involving possible 'paradominant' inheritance?
    American journal of medical genetics. Part A, 2004, Mar-15, Volume: 125A, Issue:3

    Topics: Abnormalities, Multiple; Child; Developmental Disabilities; Ectodermal Dysplasia; Genes, Dominant; H

2004
Hair and sweat glands in families with hypohidrotic ectodermal dysplasia: further characterization.
    Archives of dermatology, 2004, Volume: 140, Issue:7

    Topics: Biopsy; Case-Control Studies; Ectodermal Dysplasia; Family; Female; Hair Follicle; Hand; Humans; Mal

2004
Aplasia cutis congenita.
    Indian pediatrics, 2004, Volume: 41, Issue:9

    Topics: Bandages; Ectodermal Dysplasia; Female; Humans; Infant, Newborn; Scalp

2004
[Large scalp and skull defect in patient with aplasia cutis congenita].
    Arquivos de neuro-psiquiatria, 2004, Volume: 62, Issue:4

    Topics: Ectodermal Dysplasia; Encephalocele; Fatal Outcome; Female; Humans; Infant, Newborn; Scalp; Skull

2004
Autogenous calvarial bone graft harvest: intraoperational complications.
    The Journal of craniofacial surgery, 2005, Volume: 16, Issue:2

    Topics: Alveolar Ridge Augmentation; Bone Transplantation; Child; Craniotomy; Dental Implants; Dissection; E

2005
Congenital scalp and calvarial deficiencies: principles for classification and surgical management.
    Plastic and reconstructive surgery, 2005, Volume: 115, Issue:4

    Topics: Algorithms; Amniotic Band Syndrome; Bone Transplantation; Child; Craniofacial Abnormalities; Ectoder

2005
Early composite cranioplasty in infants with severe aplasia cutis congenita: a report of two cases.
    The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association, 2005, Volume: 42, Issue:4

    Topics: Bone Transplantation; Craniotomy; Dura Mater; Ectodermal Dysplasia; Female; Humans; Infant, Newborn;

2005
An adherent dressing for aplasia cutis congenita.
    British journal of plastic surgery, 2005, Volume: 58, Issue:8

    Topics: Bandages; Ectodermal Dysplasia; Humans; Infant, Newborn; Infant, Premature; Scalp; Treatment Outcome

2005
Light microscopic examination of scalp hair samples as an aid in the diagnosis of paediatric disorders: retrospective review of more than 300 cases from a single centre.
    Journal of clinical pathology, 2005, Volume: 58, Issue:12

    Topics: Adolescent; Adult; Age Distribution; Child; Child, Preschool; Ectodermal Dysplasia; Hair; Hair Disea

2005
Picture of the month. Cutis aplasia.
    Archives of pediatrics & adolescent medicine, 2005, Volume: 159, Issue:12

    Topics: Diagnosis, Differential; Ectodermal Dysplasia; Humans; Infant, Newborn; Male; Scalp

2005
[Scalp surgery in children: principles and therapeutic aspects].
    Revue de stomatologie et de chirurgie maxillo-faciale, 2005, Volume: 106, Issue:6

    Topics: Adolescent; Alopecia; Child; Child, Preschool; Cicatrix; Craniocerebral Trauma; Ectodermal Dysplasia

2005
The shoelace method in congenital aplasia of the scalp and skull.
    European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie, 2005, Volume: 15, Issue:6

    Topics: Diseases in Twins; Ectodermal Dysplasia; Fatal Outcome; Female; Humans; Infant, Newborn; Scalp; Scal

2005
Is surgery always necessary in the treatment of aplasia cutis congenita?
    Plastic and reconstructive surgery, 2006, Volume: 117, Issue:4

    Topics: Ectodermal Dysplasia; Female; Humans; Infant, Newborn; Scalp; Scalp Dermatoses; Surgical Flaps

2006
A nonadherent dressing for aplasia cutis congenita.
    Journal of plastic, reconstructive & aesthetic surgery : JPRAS, 2006, Volume: 59, Issue:7

    Topics: Alopecia; Bandages; Ectodermal Dysplasia; Female; Humans; Infant, Newborn; Scalp; Treatment Outcome

2006
Aplasia cutis congenita of the scalp: is there a better treatment strategy?
    Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2006, Volume: 22, Issue:10

    Topics: Ectodermal Dysplasia; Humans; Scalp

2006
Aplasia cutis congenita of the scalp: therapeutic modalities.
    Neurology India, 2006, Volume: 54, Issue:3

    Topics: Ectodermal Dysplasia; Humans; Infant; Male; Scalp; Skin Transplantation

2006
Aplasia cutis congenita of the scalp and calvarium: conservative wound management with novel wound dressing materials.
    The Journal of craniofacial surgery, 2007, Volume: 18, Issue:2

    Topics: Bandages; Bandages, Hydrocolloid; Ectodermal Dysplasia; Female; Humans; Infant, Newborn; Polyesters;

2007
Aplasia cutis congenita, congenital heart lesions, and frontonasal cysts in four successive generations.
    Clinical genetics, 2007, Volume: 71, Issue:6

    Topics: Abnormalities, Multiple; Craniofacial Abnormalities; Cysts; Ectodermal Dysplasia; Family Health; Fem

2007
Aplasia cutis associated with coarctation of the aorta: could this be an incomplete form of Adams-Oliver syndrome?
    The British journal of dermatology, 2007, Volume: 157, Issue:4

    Topics: Abnormalities, Multiple; Aortic Coarctation; Ectodermal Dysplasia; Female; Humans; Infant, Newborn;

2007
[Aplasia cutis congenita of the scalp (5 observations)].
    Archives de pediatrie : organe officiel de la Societe francaise de pediatrie, 2008, Volume: 15, Issue:4

    Topics: Bone Diseases; Consanguinity; Ectodermal Dysplasia; Humans; Infant, Newborn; Radiography; Retrospect

2008
'Membranous aplasia cutis' with hair collars. Congenital absence of skin or neuroectodermal defect?
    Archives of dermatology, 1995, Volume: 131, Issue:12

    Topics: Atrophy; Child, Preschool; Connective Tissue; Ectoderm; Ectodermal Dysplasia; Epidermis; Female; Hai

1995
[Anhidrotic ectodermal dysplasia. Disorder of the differentiation of hair follicles and sweat glands leads to abnormal keratinization].
    Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 1994, Volume: 45, Issue:6

    Topics: Antibodies, Monoclonal; Cell Differentiation; Child; Ectodermal Dysplasia; Female; Hair; Hair Diseas

1994
Reconstruction of aplasia cutis congenita of the scalp by split rib cranioplasty and a free latissimus dorsi muscle flap in a nine month old infant.
    British journal of plastic surgery, 1995, Volume: 48, Issue:7

    Topics: Bone Transplantation; Ectodermal Dysplasia; Encephalocele; Humans; Hydrocephalus; Infant; Male; Musc

1995
Scalp-ear-nipple syndrome: additional manifestations.
    American journal of medical genetics, 1994, Apr-15, Volume: 50, Issue:3

    Topics: Abnormalities, Multiple; Adult; Breast; Ear; Ectodermal Dysplasia; Female; Humans; Male; Nipples; Pe

1994
Epidermal naevi and bullous aplasia cutis congenita in a neonate.
    Journal of medical genetics, 1993, Volume: 30, Issue:11

    Topics: Ectodermal Dysplasia; Humans; Infant, Newborn; Male; Nevus, Pigmented; Scalp; Skin Diseases, Vesicul

1993
Severe skin erosions and scalp infections in AEC syndrome.
    Pediatric dermatology, 1993, Volume: 10, Issue:4

    Topics: Abnormalities, Multiple; Child; Cleft Lip; Cleft Palate; Ectodermal Dysplasia; Eyelids; Female; Huma

1993
Rapp-Hodgkin syndrome and AEC syndrome: are they the same entity?
    The British journal of dermatology, 1994, Volume: 130, Issue:1

    Topics: Cleft Palate; Ectodermal Dysplasia; Eyelids; Face; Hair; Humans; Infant; Male; Nails, Malformed; Oro

1994
Aplasia cutis congenita. Case report.
    Journal of neurosurgery, 1996, Volume: 85, Issue:1

    Topics: Adult; Ectodermal Dysplasia; Follow-Up Studies; Humans; Infant, Newborn; Scalp; Skin; Tissue Expansi

1996
[The Adams-Oliver syndrome in Spain: the epidemiological aspects].
    Anales espanoles de pediatria, 1996, Volume: 45, Issue:1

    Topics: Abnormalities, Multiple; Diagnosis, Differential; Ectodermal Dysplasia; Female; Humans; Infant, Newb

1996
Further examples of autosomal dominant transmission of nonsyndromic aplasia cutis congenita.
    American journal of medical genetics, 1997, Dec-31, Volume: 73, Issue:4

    Topics: Ectodermal Dysplasia; Female; Genes, Dominant; Humans; Infant; Male; Pedigree; Scalp

1997
Nevocellular nevus associated with alopecia presenting as aplasia cutis congenita.
    International journal of dermatology, 1998, Volume: 37, Issue:1

    Topics: Alopecia; Child; Diagnosis, Differential; Ectodermal Dysplasia; Humans; Male; Nevus; Scalp; Scalp De

1998
Surgical management of cutis aplasia with high-flow sinus pericranii.
    Pediatric neurosurgery, 1998, Volume: 28, Issue:2

    Topics: Adult; Blood Flow Velocity; Cranial Sinuses; Diagnosis, Differential; Ectodermal Dysplasia; Female;

1998
Basal cell carcinoma in aplasia cutis congenita.
    British journal of plastic surgery, 2000, Volume: 53, Issue:4

    Topics: Adult; Biopsy; Ectodermal Dysplasia; Humans; Male; Neoplasms, Basal Cell; Neoplasms, Multiple Primar

2000
Aplasia cutis congenita associated with a lipoma.
    British journal of plastic surgery, 2000, Volume: 53, Issue:4

    Topics: Ectodermal Dysplasia; Female; Humans; Infant; Lipoma; Scalp; Skin Neoplasms

2000
Large scalp and skull defect in aplasia cutis congenita.
    British journal of plastic surgery, 2000, Volume: 53, Issue:7

    Topics: Ectodermal Dysplasia; Female; Follow-Up Studies; Humans; Infant, Newborn; Plastic Surgery Procedures

2000
Large scalp and skull defects in aplasia cutis congenita.
    British journal of plastic surgery, 2001, Volume: 54, Issue:3

    Topics: Ectodermal Dysplasia; Fatal Outcome; Humans; Infant, Newborn; Male; Scalp; Surgical Flaps; Treatment

2001
Aplasia cutis congenita of the scalp: excessive bleeding and reconstructive problems.
    Annals of plastic surgery, 2001, Volume: 47, Issue:2

    Topics: Ectodermal Dysplasia; Hemorrhage; Hemostasis, Surgical; Humans; Infant; Male; Plastic Surgery Proced

2001
Aplasia cutis congenita. Report on 5 family cases involving the scalp.
    European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie, 2001, Volume: 11, Issue:4

    Topics: Ectodermal Dysplasia; Female; Humans; Infant; Infant, Newborn; Male; Scalp; Wound Healing

2001
Almost complete absence of the scalp and body hair in association with oligodontia and zygodactylous palmar triradii.
    Clinical dysmorphology, 2001, Volume: 10, Issue:4

    Topics: Abnormalities, Multiple; Adolescent; Dermatoglyphics; Ectodermal Dysplasia; Eyebrows; Eyelashes; Fam

2001
Surgical management of aplasia cutis congenita.
    Archives of surgery (Chicago, Ill. : 1960), 1976, Volume: 111, Issue:10

    Topics: Abdominal Muscles; Dura Mater; Ectodermal Dysplasia; Female; Humans; Infant; Infant, Newborn; Scalp;

1976
Failure of healing of split-skin graft donor sites in anhidrotic ectodermal dysplasia.
    Plastic and reconstructive surgery, 1979, Volume: 64, Issue:1

    Topics: Brain Neoplasms; Child; Ectodermal Dysplasia; Humans; Male; Meningioma; Scalp; Skin Transplantation;

1979
The syndrome of aplasia cutis congenita with terminal, transverse defects of limbs.
    The Journal of pediatrics, 1975, Volume: 87, Issue:1

    Topics: Abnormalities, Multiple; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Clubfoot; E

1975
Phenotypic heterogeneity among the pilosebaceous dysplasias.
    Modern problems in paediatrics, 1975, Volume: 17

    Topics: Adolescent; Alopecia; Child; Ectodermal Dysplasia; Female; Hair; Humans; Male; Orofaciodigital Syndr

1975
Multifocal aplasia cutis congenita, distal limb hemimelia, and cutis marmorata telangiectatica in a patient with Adams-Oliver syndrome.
    The British journal of dermatology, 1992, Volume: 127, Issue:2

    Topics: Abnormalities, Multiple; Ectodermal Dysplasia; Humans; Infant; Leg; Male; Scalp; Skin; Syndrome; Tel

1992
Scalp aplasia cutis congenita: closure by the L-shaped flap.
    Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 1992, Volume: 8, Issue:5

    Topics: Ectodermal Dysplasia; Female; Follow-Up Studies; Humans; Infant, Newborn; Scalp; Surgical Flaps; Sut

1992
Cutaneous scar at anterior hair line in mother and child with associated frontal bone defect in child.
    American journal of medical genetics, 1992, Sep-15, Volume: 44, Issue:2

    Topics: Abnormalities, Multiple; Adult; Cicatrix; Ectodermal Dysplasia; Female; Frontal Bone; Genes, Dominan

1992
Aplasia cutis congenita of the scalp without other defects in three siblings.
    Acta paediatrica (Oslo, Norway : 1992), 1992, Volume: 81, Issue:2

    Topics: Ectodermal Dysplasia; Female; Humans; Infant; Infant, Newborn; Male; Scalp

1992
Familial aplasia cutis congenita and coarctation of the aorta.
    American journal of medical genetics, 1992, Jul-01, Volume: 43, Issue:4

    Topics: Adult; Aortic Coarctation; Child, Preschool; Ectodermal Dysplasia; Female; Humans; Male; Scalp

1992
Large skull defect in aplasia cutis congenita treated by pericranial flap: long-term follow-up.
    Annals of plastic surgery, 1991, Volume: 26, Issue:2

    Topics: Ectodermal Dysplasia; Female; Humans; Infant; Male; Radiography; Scalp; Skull; Surgical Flaps

1991
The Rapp-Hodgkin syndrome.
    American journal of medical genetics, 1991, Volume: 38, Issue:1

    Topics: Adult; Ectodermal Dysplasia; Female; Humans; Infant, Newborn; Male; Microscopy, Electron, Scanning;

1991
Congenital scalp defects with distal limb anomalies (Adams-Oliver syndrome-McKusick 10030): further suggestion of autosomal recessive inheritance.
    American journal of medical genetics, 1989, Volume: 32, Issue:2

    Topics: Chromosome Aberrations; Chromosome Disorders; Consanguinity; Ectodermal Dysplasia; Focal Dermal Hypo

1989
Aplasia cutis congenita associated with valvular heart disease.
    Cutis, 1985, Volume: 36, Issue:1

    Topics: Ectodermal Dysplasia; Heart Septal Defects, Ventricular; Humans; Infant, Newborn; Male; Pulmonary Va

1985
Congenital absence of skin (aplasia cutis congenita).
    Archives of surgery (Chicago, Ill. : 1960), 1973, Volume: 106, Issue:5

    Topics: Debridement; Ectodermal Dysplasia; Female; Humans; Infant, Newborn; Membranes, Artificial; Scalp; Si

1973
The nevus sebaceous of Jadassohn. A neurocutaneous syndrome and a potentially premalignant lesion.
    American journal of diseases of children (1960), 1970, Volume: 120, Issue:3

    Topics: Adolescent; Adult; Child; Diagnosis, Differential; Ectodermal Dysplasia; Epilepsy; Eye Abnormalities

1970
[Netherton's syndrome. Ichthyosis-like changes in the skin and trichorrhexis invaginata. Demonstration of pathologically changed cortex keratin in the hair].
    Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 1971, Volume: 22, Issue:9

    Topics: Adolescent; Child; Child, Preschool; Ectodermal Dysplasia; Female; Hair; Humans; Ichthyosis; Infant;

1971
[Anhidrotic ectodermal dysplasia in a brother and a sister born of consanguinous parents].
    Bulletin de la Societe francaise de dermatologie et de syphiligraphie, 1969, Volume: 76, Issue:3

    Topics: Biopsy; Child; Consanguinity; Ectodermal Dysplasia; Female; Humans; Male; Scalp; Skin; Sweat Glands

1969
Congenital defect of scalp and skull in three generations of one family; case report.
    Plastic and reconstructive surgery, 1970, Volume: 46, Issue:2

    Topics: Ectodermal Dysplasia; Female; Humans; Infant, Newborn; Scalp; Skull

1970
Epidermoid and dermoid sequestration cysts.
    The American journal of roentgenology, radium therapy, and nuclear medicine, 1970, Volume: 110, Issue:1

    Topics: Adult; Aged; Anal Canal; Cecal Neoplasms; Child; Cysts; Dermoid Cyst; Ectodermal Dysplasia; Epiderma

1970
Aplasia cutis congenita.
    Archives of dermatology, 1970, Volume: 102, Issue:4

    Topics: Adolescent; Adult; Child; Child, Preschool; Ectodermal Dysplasia; Female; Humans; Infant; Infant, Ne

1970