salicylic acid has been researched along with Deficiency, Mental in 44 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).
| Excerpt | Relevance | Reference |
|---|---|---|
| "Now, he is 3 years old, and has microcephaly, moderate mental retardation, left spastic hemiplegia, and epilepsy." | 2.41 | A case of Adams-Oliver syndrome associated with acrania, microcephaly, hemiplegia, epilepsy, and mental retardation. ( Caksen, H; Kurtoğlu, S, 2000) |
| "Congenital melanocytic nevi (CMN) are nevi that are present at birth or arise within the first few weeks of life." | 1.46 | Congenital melanocytic nevus mimicking a turban tumour in an 18-year-old Filipino male. ( Cubillan, E; Sison, MEG; Tansipek, BU, 2017) |
| "Carpenter's syndrome is a relatively rare craniofacial deformity which will occasionally present to craniofacial surgeons for treatment." | 1.29 | Surgical caution with Carpenter's syndrome. ( Poole, MD, 1993) |
| "An electronystagmogram demonstrated periodic alternating nystagmus." | 1.27 | An association of subtotal cerebellar agenesis with organoid nevus--a possible new variety of neurocutaneous syndrome. ( Fukuyama, Y; Hara, M; Izumi, T; Kobayashi, N; Maeda, Y; Wang, PJ; Yajima, K, 1983) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 23 (52.27) | 18.7374 |
| 1990's | 8 (18.18) | 18.2507 |
| 2000's | 8 (18.18) | 29.6817 |
| 2010's | 3 (6.82) | 24.3611 |
| 2020's | 2 (4.55) | 2.80 |
| Authors | Studies |
|---|---|
| Ross, JB | 1 |
| Allderdice, PW | 1 |
| Shapiro, LJ | 1 |
| Aveling, J | 1 |
| Eales, BA | 1 |
| Simms, D | 1 |
| Fozia, F | 1 |
| Shah, K | 1 |
| Nazli, R | 1 |
| Khan, SA | 1 |
| Ahmad, I | 1 |
| Mohammad, N | 1 |
| Khan, S | 1 |
| Alotaibi, A | 1 |
| Sathishkumar, D | 1 |
| Ogboli, M | 1 |
| Moss, C | 1 |
| Sison, MEG | 1 |
| Cubillan, E | 1 |
| Tansipek, BU | 1 |
| Huang, X | 2 |
| Yuan, Q | 1 |
| Luo, Q | 1 |
| Zeng, H | 1 |
| Zheng, X | 1 |
| Yu, Y | 1 |
| Wu, Y | 1 |
| Curatolo, P | 2 |
| Lo-Castro, A | 1 |
| Pinci, M | 1 |
| Moavero, R | 1 |
| Bombardieri, R | 1 |
| Hartman, EC | 1 |
| Gilles, E | 1 |
| McComas, JJ | 1 |
| Danov, SE | 1 |
| Symons, FJ | 1 |
| Blyth, M | 1 |
| Baralle, D | 1 |
| KRATTER, FE | 1 |
| BERG, JM | 1 |
| WINDRATH-SCOTT, A | 1 |
| AKESSON, HO | 3 |
| Schöttler, L | 1 |
| Denisjuk, N | 1 |
| Körber, A | 1 |
| Grabbe, S | 1 |
| Dissemond, J | 1 |
| Wang, PJ | 1 |
| Maeda, Y | 1 |
| Izumi, T | 1 |
| Yajima, K | 1 |
| Hara, M | 1 |
| Kobayashi, N | 1 |
| Fukuyama, Y | 1 |
| Guidetti, V | 1 |
| Garcovich, A | 1 |
| Paolella, A | 1 |
| Bamforth, JS | 1 |
| Kaurah, P | 1 |
| Byrne, J | 1 |
| Ferreira, P | 1 |
| Zoll, B | 1 |
| Wolf, J | 1 |
| Lensing-Hebben, D | 1 |
| Pruggmayer, M | 1 |
| Thorpe, B | 1 |
| Poole, MD | 1 |
| Striano, S | 1 |
| Ruosi, P | 1 |
| Guzzetta, V | 1 |
| Perone, L | 1 |
| Manto, A | 1 |
| Cirillo, S | 1 |
| Chang, GY | 1 |
| Farah, S | 1 |
| Farag, T | 1 |
| Sabry, MA | 1 |
| Simeonov, ST | 1 |
| al-Khattam, S | 1 |
| Abulhassan, SJ | 1 |
| Quasrawi, B | 1 |
| al-Busairi, W | 1 |
| al-Awadi, SA | 1 |
| Koivisto, PA | 1 |
| Koivisto, H | 1 |
| Haapala, K | 1 |
| Simola, KO | 1 |
| Koizumi, T | 1 |
| Caksen, H | 1 |
| Kurtoğlu, S | 1 |
| Fryns, JP | 2 |
| de Cock, P | 1 |
| Filosto, M | 1 |
| Tonin, P | 1 |
| Vattemi, G | 1 |
| Bongiovanni, LG | 1 |
| Rizzuto, N | 1 |
| Tomelleri, G | 1 |
| Keller, K | 1 |
| Williams, C | 1 |
| Seagle, B | 1 |
| Campbell, WW | 1 |
| Buda, FB | 1 |
| Sorensen, G | 1 |
| Katalin, K | 1 |
| Magdolna, M | 1 |
| Péter, L | 1 |
| Mohanty, S | 1 |
| Rao, CJ | 1 |
| Iivanainen, M | 3 |
| Arho, P | 1 |
| Schepis, C | 1 |
| Palazzo, R | 1 |
| Cannavo, SP | 1 |
| Ragusa, RM | 1 |
| Barletta, C | 1 |
| Spina, E | 1 |
| Diven, DG | 1 |
| Solomon, AR | 1 |
| McNeely, MC | 1 |
| Font, RL | 1 |
| Felding, I | 1 |
| Feingold, M | 1 |
| Uyama, E | 1 |
| Teramoto, H | 1 |
| Hashimoto, Y | 1 |
| Okamoto, H | 1 |
| Araki, S | 1 |
| Buttiëns, M | 1 |
| Jonckheere, P | 1 |
| Brouckmans-Buttiëns, K | 1 |
| Van den Berghe, H | 1 |
| Berger, H | 1 |
| Tsuang, MT | 1 |
| Lin, SN | 1 |
| Silvers, DN | 1 |
| Cox, RP | 1 |
| Balis, ME | 1 |
| Dancis, J | 1 |
| Kostiainen, E | 1 |
| Bianchine, JW | 1 |
| Muller, SA | 1 |
| Winkelmann, RK | 1 |
| Palo, J | 1 |
3 reviews available for salicylic acid and Deficiency, Mental
| Article | Year |
|---|---|
Trisomy 13 (Patau syndrome) with an 11-year survival.
Topics: Abnormalities, Multiple; Adult; Brain; Child; Child, Preschool; Chromosomes, Human, Pair 13; Female; | 1993 |
[Johanson-Blizzard syndrome].
Topics: Abnormalities, Multiple; Diagnosis, Differential; Exocrine Pancreatic Insufficiency; Growth Disorder | 2000 |
A case of Adams-Oliver syndrome associated with acrania, microcephaly, hemiplegia, epilepsy, and mental retardation.
Topics: Abnormalities, Multiple; Consanguinity; Ectodermal Dysplasia; Epilepsy, Tonic-Clonic; Fingers; Growt | 2000 |
1 trial available for salicylic acid and Deficiency, Mental
| Article | Year |
|---|---|
[Clinical efficacy on mental retardation in the children treated with JIN's three scalp needling therapy and the training for cognitive and perceptual disturbance].
Topics: Acupuncture Therapy; Child; Child, Preschool; Cognition; Female; Humans; Intellectual Disability; In | 2015 |
40 other studies available for salicylic acid and Deficiency, Mental
| Article | Year |
|---|---|
Familial X-linked ichthyosis, steroid sulfatase deficiency, mental retardation, and nullisomy for Xp223-pter.
Topics: Adult; Child; Chromosome Aberrations; Chromosome Deletion; Female; Gels; Genetic Linkage; Humans; Ic | 1985 |
Novel splicing-site mutation in DCAF17 gene causing Woodhouse-Sakati syndrome in a large consanguineous family.
Topics: Adolescent; Alopecia; Arrhythmias, Cardiac; Basal Ganglia Diseases; Child; Consanguinity; Diabetes M | 2022 |
Classification of aplasia cutis congenita: a 25-year review of cases presenting to a tertiary paediatric dermatology department.
Topics: Abnormalities, Multiple; Child; Child, Preschool; Cleft Palate; Dermatology; Ectodermal Dysplasia; E | 2020 |
Congenital melanocytic nevus mimicking a turban tumour in an 18-year-old Filipino male.
Topics: Adolescent; Diagnosis, Differential; Head and Neck Neoplasms; Humans; Intellectual Disability; Male; | 2017 |
Neuroimaging findings of Sturge-Weber Syndrome in a child with Tuberous Sclerosis.
Topics: Adolescent; Brain; Comorbidity; Epilepsy; Female; Heart Defects, Congenital; Humans; Intellectual Di | 2009 |
Clinical observation of self-injurious behavior correlated with changes in scalp morphology in a child with congenital hydrocephalus.
Topics: Cerebrospinal Fluid Shunts; Child; Craniofacial Abnormalities; Craniotomy; Female; Humans; Hydroceph | 2008 |
Anophthalmia in fronto-facial-nasal dysplasia.
Topics: Abnormalities, Multiple; Adolescent; Anophthalmos; Autistic Disorder; Cleft Lip; Cleft Palate; Crani | 2011 |
The incidence of cutis verticis gyrata in three low-grade mental defectives.
Topics: Connective Tissue Diseases; Disease; Humans; Incidence; Intellectual Disability; Medical Records; Sc | 1958 |
Cutis verticis gyrata with particular reference to its association with mental subnormality.
Topics: Connective Tissue Diseases; Humans; Intellectual Disability; Mental Disorders; Scalp; Skin Diseases | 1962 |
CUTIS VERTICIS GYRATA AND MENTAL DEFICIENCY IN SWEDEN. I. EPIDEMIOLOGIC AND CLINICAL ASPECTS.
Topics: 17-Ketosteroids; Acromegaly; Adrenal Cortex Hormones; Castration; Cerebral Palsy; Chromatography; Co | 1964 |
CUTIS VERTICIS GYRATA AND MENTAL DEFICIENCY IN SWEDEN. II. GENETIC ASPECTS.
Topics: Congenital Abnormalities; Connective Tissue Diseases; Genetics, Medical; Humans; Intellectual Disabi | 1965 |
CUTIS VERTICIS GYRATA THYROAPLASIA AND MENTAL DEFICIENCY.
Topics: Connective Tissue Diseases; Genes; Genetics, Medical; Humans; Intellectual Disability; Pathology; Sc | 1965 |
[Asymptomatic cerebriform folds of the scalp. Diagnosis: primary Cutis verticis gyrata (CVG)].
Topics: Adult; Asphyxia Neonatorum; Biopsy; Chromosome Aberrations; Chromosomes, Human, X; Diagnosis, Differ | 2007 |
An association of subtotal cerebellar agenesis with organoid nevus--a possible new variety of neurocutaneous syndrome.
Topics: Adolescent; Cerebellum; Electronystagmography; Female; Humans; Intellectual Disability; Nevus; Nysta | 1983 |
[Epidermal nervus syndrome].
Topics: Cerebral Palsy; Facial Neoplasms; Facial Paralysis; Female; Humans; Infant; Intellectual Disability; | 1982 |
Adams Oliver syndrome: a family with extreme variability in clinical expression.
Topics: Abnormalities, Multiple; Adult; Brain; Bronchi; Epilepsy; Female; Heart Defects, Congenital; Humans; | 1994 |
Surgical caution with Carpenter's syndrome.
Topics: Acrocephalosyndactylia; Blood Loss, Surgical; Child, Preschool; Cranial Sinuses; Frontal Bone; Human | 1993 |
Cutis verticis gyrata--mental deficiency syndrome: a patient with drug-resistant epilepsy and polymicrogyria.
Topics: Adult; Chromosomes, Human, Pair 16; Chromosomes, Human, Pair 3; Epilepsy; Humans; Intellectual Disab | 1996 |
Cutis verticis gyrata, underrecognized neurocutaneous syndrome.
Topics: Adult; Epilepsy; Humans; Intellectual Disability; Magnetic Resonance Imaging; Male; Scalp; Syndrome | 1996 |
Cutis verticis gyrata-mental deficiency syndrome: report of a case with unusual neuroradiological findings.
Topics: Adult; Brain; Chromosome Inversion; Epilepsy; Humans; Intellectual Disability; Magnetic Resonance Im | 1998 |
A de novo deletion of chromosome 15(q15.2q21.2) in a dysmorphic, mentally retarded child with congenital scalp defect.
Topics: Chromosome Banding; Chromosome Deletion; Chromosomes, Human, Pair 15; Facies; Humans; Infant, Newbor | 1999 |
MCA/MR syndrome with occipital scalp defect and valvular pulmonary stenosis: a cryptic 7pter duplication/18qter deficiency.
Topics: Child; Child, Preschool; Chromosomes, Human, Pair 18; Chromosomes, Human, Pair 7; Humans; Intellectu | 2001 |
Cutis verticis gyrata, mental retardation and Lennox-Gastaut syndrome: a case report.
Topics: Adult; Electroencephalography; Epilepsy, Absence; Humans; Intellectual Disability; Magnetic Resonanc | 2001 |
Klinefelter syndrome and cutis verticis gyrata.
Topics: Acromegaly; Adult; Diagnosis, Differential; Follow-Up Studies; Humans; Intellectual Disability; Kary | 2001 |
Linear nevus sebaceous syndrome: neurological aspects documented by brain scans correlated with developmental history and radiographic studies.
Topics: Brain Diseases; Child; Female; Humans; Intellectual Disability; Nevus; Scalp; Sebaceous Gland Neopla | 1978 |
[Indication and value of trichoglyphic examinations].
Topics: Child, Preschool; Female; Gestational Age; Hair; Humans; Intellectual Disability; Male; Microcephaly | 1977 |
A large cirsoid aneurysm of the scalp associated with epilepsy.
Topics: Aneurysm; Epilepsy; Female; Humans; Infant; Intellectual Disability; Scalp | 1976 |
Skin thickness in cutis verticis gyrata and mental retardation syndrome.
Topics: Adult; Female; Humans; Hypertrophy; Intellectual Disability; Male; Scalp; Skin Diseases; Skinfold Th | 1976 |
Prevalence of primary cutis verticis gyrata in a psychiatric population: association with chromosomal fragile sites.
Topics: Adult; Aged; Aged, 80 and over; Chromosome Fragile Sites; Chromosome Fragility; Female; Fragile X Sy | 1990 |
Nevus sebaceus associated with major ophthalmologic abnormalities.
Topics: Adolescent; Choristoma; Choroid; Coloboma; Eye Abnormalities; Female; Humans; Intellectual Disabilit | 1987 |
Picture of the month. Cutis verticis gyrata.
Topics: Abnormalities, Multiple; Brain; Humans; Infant; Infant, Newborn; Intellectual Disability; Male; Scal | 1988 |
[Two siblings of familial spastic paraplegia with cutis verticis gyrata and mental retardation].
Topics: Adult; Humans; Intellectual Disability; Male; Muscle Spasticity; Paraplegia; Scalp | 1988 |
Scalp defect associated with postaxial polydactyly: confirmation of a distinct entity with autosomal dominant inheritance.
Topics: Adolescent; Fingers; Genes, Dominant; Humans; Intellectual Disability; Male; Radiography; Scalp; Sku | 1985 |
On the electroencephalogram of man. Third report.
Topics: Adolescent; Adult; Anesthesia; Brain Injuries; Cerebral Cortex; Cerebral Hemorrhage; Cerebrovascular | 1969 |
Cutis verticis gyrata in a Chinese mental defective.
Topics: Adult; Cerebral Palsy; Congenital Abnormalities; Electroencephalography; Epilepsy, Tonic-Clonic; Hum | 1974 |
Detection of the heterozygote in Lesch-Nyhan disease by hair-root analysis.
Topics: Adenosine Monophosphate; Athetosis; Clinical Enzyme Tests; Culture Techniques; Female; Fibroblasts; | 1972 |
The electrophoretic pattern of cerebrospinal fluid proteins in the cutis verticis gyrata and mental retardation syndrome.
Topics: Adolescent; Adult; Albumins; Blood Protein Electrophoresis; Cerebral Palsy; Cerebral Ventricles; Cer | 1974 |
The nevus sebaceous of Jadassohn. A neurocutaneous syndrome and a potentially premalignant lesion.
Topics: Adolescent; Adult; Child; Diagnosis, Differential; Ectodermal Dysplasia; Epilepsy; Eye Abnormalities | 1970 |
Trichotillomania. A clinicopathologic study of 24 cases.
Topics: Adolescent; Adult; Alopecia; Biopsy; Child; Child, Preschool; Eyebrows; Eyelashes; Female; Hair; Hum | 1972 |
The cutis verticis gyrata and mental retardation syndrome in a 4-year-old boy.
Topics: Abnormalities, Multiple; Child, Preschool; Humans; Intellectual Disability; Male; Osteoarthropathy, | 1971 |