Page last updated: 2024-10-17

salicylic acid and Hypotrichosis

salicylic acid has been researched along with Hypotrichosis in 39 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).

Hypotrichosis: Presence of less than the normal amount of hair. (Dorland, 27th ed)

Research Excerpts

ExcerptRelevanceReference
"Gentamicin was further shown to rescue corneodesmosin translation in primary keratinocytes obtained from a patient with HSS."6.94Treatment of hereditary hypotrichosis simplex of the scalp with topical gentamicin. ( Bochner, R; Malki, L; Pavlovsky, M; Peled, A; Pichinuk, E; Samuelov, L; Sarig, O; Sprecher, E; Weil, M, 2020)
"Gentamicin was further shown to rescue corneodesmosin translation in primary keratinocytes obtained from a patient with HSS."2.94Treatment of hereditary hypotrichosis simplex of the scalp with topical gentamicin. ( Bochner, R; Malki, L; Pavlovsky, M; Peled, A; Pichinuk, E; Samuelov, L; Sarig, O; Sprecher, E; Weil, M, 2020)
"Ichthyosis is a heterogeneous group of skin disorders characterized by abnormal epidermal scaling."1.31Homozygosity mapping of a locus for a novel syndromic ichthyosis to chromosome 3q27-q28. ( Baala, L; Courtois, G; De Prost, Y; Hadchouel, M; Hadj-Rabia, S; Hamel-Teillac, D; Jacquemin, E; Leal, SM; Lyonnet, S; Munnich, A; Prost, C; Sefiani, A; Vabres, P, 2002)
"Gonosomal aberrations such as Turner's syndrome are frequently associated with autoimmune diseases or with serological markers for autoimmune diseases."1.29[Alopecia areata and diffuse hypotrichosis associated with Ullrich-Turner syndrome. Presentation of 4 patients]. ( Gollnick, H; Müller, R; Orfanos, CE; Reupke, HJ; Tebbe, B, 1993)
"A case of naevoid hypotrichosis affecting two symmetrical areas in the parietal regions is described."1.27Focal naevoid hypotrichosis. ( Barth, JH; Dawber, RP, 1987)

Research

Studies (39)

TimeframeStudies, this research(%)All Research%
pre-19907 (17.95)18.7374
1990's4 (10.26)18.2507
2000's10 (25.64)29.6817
2010's11 (28.21)24.3611
2020's7 (17.95)2.80

Authors

AuthorsStudies
López-Balboa, P1
Martos-Cabrera, L1
Ramírez-Lluch, M1
Noguera-Morel, L1
Ortiz-Cabrera, NV1
González-Sarmiento, R1
Torrelo, A1
Hernández-Martín, Á1
Vastarella, M1
Martora, F1
Ocampo-Garza, S1
Patri, A1
Battista, T1
Nappa, P1
Fabbrocini, G1
Cantelli, M1
Rayinda, T1
McSweeney, SM1
Lalagianni, N1
Liu, L1
Guy, A1
Fenton, D1
Stefanato, CM1
Dand, N1
McGrath, JA1
Tziotzios, C1
de Abreu, EP1
Rocha, VB1
Queiroz de Melo, RF1
Pereira, LB1
Peled, A1
Samuelov, L1
Sarig, O1
Bochner, R1
Malki, L1
Pavlovsky, M1
Pichinuk, E1
Weil, M1
Sprecher, E2
Kibbi, N1
Rajan, N1
Taki, T1
Tanahashi, K1
Takeichi, T1
Yoshikawa, T1
Murase, Y1
Sugiura, K1
Akiyama, M1
Farah, RS1
Holahan, HM1
Moye, MS1
Stone, MS1
Swick, BL1
Huang, H1
Sun, J1
Fu, L1
Wu, J1
Guo, H1
Yang, C1
Zheng, X1
Tang, H1
Sun, L1
Zhang, X1
Liu, LH1
Wang, JW1
Chen, G1
Chang, RX1
Zhou, Y1
Tang, HY1
Zhu, J1
Wang, PG1
Yang, S1
Zhang, XJ1
Kolb-Mäurer, A1
Betz, RC5
Hamm, H1
Doh, EJ1
Yoon, HS1
Cho, S1
Park, HS1
Gentile, P1
Garcovich, S1
Bielli, A1
Scioli, MG1
Orlandi, A1
Cervelli, V1
Barrón-Hernández, YL1
Tosti, A1
Düzenli, S1
Redler, S1
Müller, M1
Polat, M1
Dogruer, D1
Pasternack, SM1
Shimomura, Y1
Agalliu, D1
Vonica, A1
Luria, V1
Wajid, M1
Baumer, A1
Belli, S1
Petukhova, L1
Schinzel, A1
Brivanlou, AH1
Barres, BA1
Christiano, AM2
Caubet, C1
Bousset, L1
Clemmensen, O1
Sourigues, Y1
Bygum, A3
Chavanas, S1
Coudane, F1
Hsu, CY1
Melki, R1
Simon, M2
Serre, G2
Nahum, S1
Morice-Picard, F1
Taieb, A1
Huang, XS1
Jiang, HO1
Quan, QL1
Baala, L1
Hadj-Rabia, S1
Hamel-Teillac, D1
Hadchouel, M1
Prost, C1
Leal, SM1
Jacquemin, E1
Sefiani, A1
De Prost, Y1
Courtois, G1
Munnich, A1
Lyonnet, S1
Vabres, P1
Levy-Nissenbaum, E1
Frydman, M1
Lahat, H1
Bakhan, T1
Goldman, B1
Pierick, M1
Hillmer, AM1
Jonca, N1
Toribio, J3
Kruse, R2
Dewald, G1
Cichon, S2
Kubisch, C1
Guerrin, M1
Nöthen, MM2
Pras, E1
Green, J1
Fitzpatrick, E1
de Berker, D1
Forrest, SM1
Sinclair, RD1
Sinclair, R1
Schaffer, JV1
Bazzi, H1
Vitebsky, A1
Witkiewicz, A1
Kovich, OI1
Kamino, H1
Shapiro, LS1
Amin, SP1
Orlow, SJ1
Kanitakis, J1
Tebbe, B1
Gollnick, H1
Müller, R1
Reupke, HJ1
Orfanos, CE1
Rodríguez Díaz, E1
Fernández Blasco, G1
Martín Pascual, A1
Armijo, M1
Glaessl, A1
Hohenlautner, U1
Landthaler, M1
Vogt, T1
Lee, YA1
Brandrup, F2
Bernal, AI1
Alvarez, JI1
Kukuk, GM1
Ibsen, HH2
Rasmussen, HB1
Wienker, TF1
Reis, A1
Propping, P1
Atasua, M1
Dumlu, A1
Ozbayrak, S1
Spiegl, B1
Hundeiker, M1
Lazović-Tepavac, O1
Gaćinović-Kostanjsek, Z1
Korić-Gackić, A1
Salamon, T1
Clemmensen, OJ1
Hess, RO1
Uno, H1
Barth, JH1
Dawber, RP1
Dekio, S1
Nagashima, T1
Watanabe, Y1
Jidoi, J1
Kohn, G1
Metzker, A1
Wirth, G1
Bindewald, I1
Küster, W1
Goerz, G1
Quiñones, PA1

Clinical Trials (2)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Biocellular Regenerative Therapy in Treating Scaring Alopecias and Alopecia Areata: Use of High Density Platelet-Rich Plasma Concentrates and Cell-Enriched Emulsified Adipose-Derived Tissue Stromal Vascular Fraction (AD-tSVF)[NCT03078686]60 participants (Anticipated)Interventional2017-02-17Recruiting
Evaluating the Efficacy of Different Platelet Rich Plasma (PRP) Treatment Regimens in the Management of Androgenetic Alopecia: an Investigator-initiated, Single-center, Single-blinded, Prospective, Randomized Clinical Trial[NCT02999737]Phase 440 participants (Actual)Interventional2016-11-30Active, not recruiting
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Reviews

3 reviews available for salicylic acid and Hypotrichosis

ArticleYear
Odd-looking hair and progressive alopecia in mother and son.
    JAMA dermatology, 2014, Volume: 150, Issue:5

    Topics: Adult; Alopecia; Biopsy, Needle; Disease Progression; Female; Follow-Up Studies; Hair; Heterozygote;

2014
Bimatoprost for the treatment of eyelash, eyebrow and scalp alopecia.
    Expert opinion on investigational drugs, 2017, Volume: 26, Issue:4

    Topics: Alopecia; Bimatoprost; Eyebrows; Eyelashes; Humans; Hypotrichosis; Scalp

2017
Sporadic Bazex-Dupré-Christol-like syndrome: early onset basal cell carcinoma, hypohidrosis, hypotrichosis, and prominent milia.
    Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.], 2000, Volume: 26, Issue:2

    Topics: Acneiform Eruptions; Adult; Carcinoma, Basal Cell; Female; Humans; Hypohidrosis; Hypotrichosis; Neop

2000

Trials

3 trials available for salicylic acid and Hypotrichosis

ArticleYear
Treatment of hereditary hypotrichosis simplex of the scalp with topical gentamicin.
    The British journal of dermatology, 2020, Volume: 183, Issue:1

    Topics: Gentamicins; Glycoproteins; Humans; Hypotrichosis; Intercellular Signaling Peptides and Proteins; Pe

2020
Association of Topical Minoxidil With Autosomal Recessive Woolly Hair/Hypotrichosis Caused by LIPH Pathogenic Variants.
    JAMA dermatology, 2020, 10-01, Volume: 156, Issue:10

    Topics: Administration, Topical; Adolescent; Child; Child, Preschool; Female; Hair; Hair Diseases; Hair Foll

2020
The Effect of Platelet-Rich Plasma in Hair Regrowth: A Randomized Placebo-Controlled Trial.
    Stem cells translational medicine, 2015, Volume: 4, Issue:11

    Topics: Adult; Follow-Up Studies; Hair Follicle; Humans; Hypotrichosis; Male; Middle Aged; Platelet-Rich Pla

2015
The Effect of Platelet-Rich Plasma in Hair Regrowth: A Randomized Placebo-Controlled Trial.
    Stem cells translational medicine, 2015, Volume: 4, Issue:11

    Topics: Adult; Follow-Up Studies; Hair Follicle; Humans; Hypotrichosis; Male; Middle Aged; Platelet-Rich Pla

2015
The Effect of Platelet-Rich Plasma in Hair Regrowth: A Randomized Placebo-Controlled Trial.
    Stem cells translational medicine, 2015, Volume: 4, Issue:11

    Topics: Adult; Follow-Up Studies; Hair Follicle; Humans; Hypotrichosis; Male; Middle Aged; Platelet-Rich Pla

2015
The Effect of Platelet-Rich Plasma in Hair Regrowth: A Randomized Placebo-Controlled Trial.
    Stem cells translational medicine, 2015, Volume: 4, Issue:11

    Topics: Adult; Follow-Up Studies; Hair Follicle; Humans; Hypotrichosis; Male; Middle Aged; Platelet-Rich Pla

2015

Other Studies

33 other studies available for salicylic acid and Hypotrichosis

ArticleYear
Hypotrichosis simplex of the scalp and peeling skin disease, two sides of the same coin.
    Journal of the European Academy of Dermatology and Venereology : JEADV, 2022, Volume: 36, Issue:10

    Topics: Humans; Hypotrichosis; Pedigree; Scalp; Skin Abnormalities; Skin Diseases

2022
Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors.
    Dermatologic therapy, 2022, Volume: 35, Issue:9

    Topics: Alopecia; Humans; Hypotrichosis; Intercellular Signaling Peptides and Proteins; Minoxidil; Scalp

2022
Familial hypotrichosis simplex of the scalp associated with a novel heterozygous nonsense variant in CDSN.
    Clinical and experimental dermatology, 2023, 04-27, Volume: 48, Issue:5

    Topics: Codon, Nonsense; Humans; Hypotrichosis; Intercellular Signaling Peptides and Proteins; Pedigree; Sca

2023
Hypotrichosis and Hair Loss on the Occipital Scalp.
    Cutis, 2023, Volume: 112, Issue:3

    Topics: Alopecia; Hair; Humans; Hypotrichosis; Pedigree; Scalp

2023
Reading through genetic 'stop signs': a therapeutic strategy in genetic skin disease.
    The British journal of dermatology, 2020, Volume: 183, Issue:1

    Topics: Gentamicins; Humans; Hypotrichosis; Reading; Scalp; Skin Diseases, Genetic

2020
Hereditary hypotrichosis simplex of the scalp.
    Cutis, 2017, Volume: 100, Issue:1

    Topics: Alopecia; Child; Diagnosis, Differential; Female; Humans; Hypotrichosis; Pedigree; Scalp

2017
A novel insertion mutation of CDSN responsible for hypotrichosis simplex of scalp in a Chinese family.
    Clinical and experimental dermatology, 2018, Volume: 43, Issue:6

    Topics: Alopecia; China; Genetic Variation; Glycoproteins; Humans; Hypotrichosis; Intercellular Signaling Pe

2018
Homozygous missense mutation in the LIPH gene causing autosomal recessive hypotrichosis simplex in a Chinese patient.
    The Journal of dermatology, 2014, Volume: 41, Issue:1

    Topics: Alopecia; Asian People; Child; China; Homozygote; Humans; Hypotrichosis; Lipase; Male; Mutation, Mis

2014
Occipital neuralgia after scalp biopsy and curettage.
    The British journal of dermatology, 2015, Volume: 173, Issue:6

    Topics: Biopsy; Curettage; Female; Headache Disorders; Humans; Hypotrichosis; Middle Aged; Neuralgia; Scalp;

2015
Identification of a U2HR gene mutation in Turkish families with Marie Unna hereditary hypotrichosis.
    Clinical and experimental dermatology, 2009, Volume: 34, Issue:8

    Topics: Chromosome Mapping; Genes, Recessive; Genotype; Hair; Humans; Hypotrichosis; Male; Middle Aged; Pedi

2009
APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex.
    Nature, 2010, Apr-15, Volume: 464, Issue:7291

    Topics: Animals; beta Catenin; Cell Differentiation; Cell Line; Cell Proliferation; Chick Embryo; Chromosome

2010
A new amyloidosis caused by fibrillar aggregates of mutated corneodesmosin.
    FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2010, Volume: 24, Issue:9

    Topics: Aged; Amyloidosis; Cells, Cultured; Circular Dichroism; Glycoproteins; Humans; Hypotrichosis; In Vit

2010
A novel mutation in LPAR6 causes autosomal recessive hypotrichosis of the scalp.
    Clinical and experimental dermatology, 2011, Volume: 36, Issue:2

    Topics: Adolescent; Amino Acid Substitution; DNA Mutational Analysis; Female; Genotype; Humans; Hypotrichosi

2011
[Clinical investigation of a Chinese family with hypotrichosis simplex of the scalp and mutational analysis of CDSN gene].
    Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, 2012, Volume: 29, Issue:4

    Topics: Alopecia; China; Codon, Nonsense; Female; Glycoproteins; Humans; Hypotrichosis; Intercellular Signal

2012
Homozygosity mapping of a locus for a novel syndromic ichthyosis to chromosome 3q27-q28.
    The Journal of investigative dermatology, 2002, Volume: 119, Issue:1

    Topics: Adolescent; Child; Child, Preschool; Cholangitis, Sclerosing; Chromosome Mapping; Chromosomes, Human

2002
Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin.
    Nature genetics, 2003, Volume: 34, Issue:2

    Topics: Base Sequence; Child; Chromosomes, Human, Pair 6; Codon, Nonsense; DNA; Genetic Linkage; Glycoprotei

2003
Progressive patterned scalp hypotrichosis, with wiry hair, onycholysis, and intermittently associated cleft lip and palate: clinical and genetic distinction from Marie Unna.
    The journal of investigative dermatology. Symposium proceedings, 2003, Volume: 8, Issue:1

    Topics: Adolescent; Adult; Cleft Lip; Cleft Palate; Diagnosis, Differential; Female; Hair; Humans; Hypotrich

2003
Chronic telogen effluvium: a study of 5 patients over 7 years.
    Journal of the American Academy of Dermatology, 2005, Volume: 52, Issue:2 Suppl 1

    Topics: Adolescent; Adult; Alopecia; Biopsy; Chronic Disease; Diagnosis, Differential; Female; Follow-Up Stu

2005
Mutations in the desmoglein 4 gene underlie localized autosomal recessive hypotrichosis with monilethrix hairs and congenital scalp erosions.
    The Journal of investigative dermatology, 2006, Volume: 126, Issue:6

    Topics: Amino Acid Sequence; Child, Preschool; Desmogleins; DNA Mutational Analysis; Female; Hair; Hair Dise

2006
Hypotrichosis simplex of the scalp.
    Journal of the European Academy of Dermatology and Venereology : JEADV, 2007, Volume: 21, Issue:10

    Topics: Chromosomes, Human, Pair 6; Genes, Dominant; Hair Follicle; Humans; Hypotrichosis; Male; Pedigree; S

2007
[Alopecia areata and diffuse hypotrichosis associated with Ullrich-Turner syndrome. Presentation of 4 patients].
    Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 1993, Volume: 44, Issue:10

    Topics: Adult; Alopecia Areata; Female; Hair; Humans; Hypotrichosis; Scalp; Turner Syndrome

1993
Hereditary hypotrichosis simplex of the scalp.
    Dermatology (Basel, Switzerland), 1995, Volume: 191, Issue:2

    Topics: Adolescent; Biopsy; Female; Genes, Dominant; Hair; Humans; Hypotrichosis; Microscopy, Electron, Scan

1995
A gene for hypotrichosis simplex of the scalp maps to chromosome 6p21.3.
    American journal of human genetics, 2000, Volume: 66, Issue:6

    Topics: Adolescent; Age of Onset; Chromosome Mapping; Chromosomes, Human, Pair 6; Female; Genes, Dominant; H

2000
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
[Congenital hereditary hypotrychosis. Generalized autosomal dominant hypotrichosis with pili torti (hypotrichosis congenita hereditaria Marie Unna)].
    Fortschritte der Medizin, 1979, Nov-22, Volume: 97, Issue:44

    Topics: Adolescent; Alopecia; Chromosome Aberrations; Chromosome Disorders; Genes, Dominant; Hair; Humans; H

1979
[A case of congenital hypotrichosis with hair abnormalities, scar-like changes of the scalp, corneal changes and a congenital heart defect].
    Dermatologische Monatschrift, 1978, Volume: 164, Issue:5

    Topics: Abnormalities, Multiple; Alopecia; Child, Preschool; Female; Hair; Heart Defects, Congenital; Humans

1978
Familial hypotrichosis of the scalp. Autosomal dominant inheritance in four generations.
    Acta dermato-venereologica, 1991, Volume: 71, Issue:4

    Topics: Adult; Age Factors; Aged; Aged, 80 and over; Biopsy; Child; Female; Genes, Dominant; Hair; Humans; H

1991
Hereditary hypotrichosis of the scalp.
    American journal of medical genetics, 1991, May-01, Volume: 39, Issue:2

    Topics: Adult; Child, Preschool; Female; Genes, Dominant; Hair; Humans; Hypotrichosis; Male; Microscopy, Ele

1991
Focal naevoid hypotrichosis.
    Acta dermato-venereologica, 1987, Volume: 67, Issue:2

    Topics: Alopecia; Child, Preschool; Humans; Hypotrichosis; Male; Nevus, Pigmented; Scalp; Skin Neoplasms

1987
Hypotrichosis with keratosis pilaris: electrophoretical study of hair fibrous proteins from a patient.
    Dermatologica, 1989, Volume: 179, Issue:3

    Topics: Adult; Alopecia; Amino Acids; Darier Disease; Electrophoresis, Gel, Two-Dimensional; Hair; Humans; H

1989
Hereditary hypotrichosis simplex of the scalp.
    Clinical genetics, 1987, Volume: 32, Issue:2

    Topics: Adult; Alopecia; Child; Female; Genes, Dominant; Humans; Hypotrichosis; Israel; Jews; Male; Pedigree

1987
[Hypotrichosis congenita hereditaria Maria Unna].
    Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 1985, Volume: 36, Issue:10

    Topics: Adult; Alopecia; Child, Preschool; Female; Hair; Humans; Hypotrichosis; Microscopy, Electron, Scanni

1985
Hereditary hypotrichosis simplex of the scalp. Evidence for autosomal dominant inheritance.
    The British journal of dermatology, 1974, Volume: 91, Issue:6

    Topics: Adolescent; Adult; Age Factors; Alopecia; Child; Child, Preschool; Chromatography; Female; Genes, Do

1974