"Hair Diseases" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Diseases affecting the orderly growth and persistence of hair.
| Descriptor ID |
D006201
|
| MeSH Number(s) |
C17.800.329
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Hair Diseases".
Below are MeSH descriptors whose meaning is more specific than "Hair Diseases".
This graph shows the total number of publications written about "Hair Diseases" by people in this website by year, and whether "Hair Diseases" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2010 | 1 | 0 | 1 |
| 2011 | 1 | 0 | 1 |
| 2012 | 1 | 0 | 1 |
| 2015 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
| 2017 | 1 | 0 | 1 |
| 2018 | 0 | 1 | 1 |
| 2019 | 1 | 0 | 1 |
| 2022 | 3 | 0 | 3 |
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Below are the most recent publications written about "Hair Diseases" by people in Profiles.
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Assessment of the Genetic Spectrum of Uncombable Hair Syndrome in a Cohort of 107 Individuals. JAMA Dermatol. 2022 11 01; 158(11):1245-1253.
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A new de novo heterozygous missense mutation in the desmoplakin gene, causing Naxos and Carvajal disease, associating oligodontia and nail fragility. Clin Exp Dermatol. 2022 Jul; 47(7):1424-1426.
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A girl with unruly locks: molecular genetics makes a diagnosis of uncombable hair syndrome. Lancet. 2022 03 12; 399(10329):1079.
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[Hair anomalies in syndromic disorders]. Hautarzt. 2019 Jul; 70(7):514-519.
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Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex. Am J Hum Genet. 2018 11 01; 103(5):777-785.
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Congenital Anonychia and Uncombable Hair Syndrome: Coinheritance of Homozygous Mutations in RSPO4 and PADI3. J Invest Dermatol. 2017 05; 137(5):1176-1179.
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Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome. Am J Hum Genet. 2016 Dec 01; 99(6):1292-1304.
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Identification of a novel mutation in RIPK4 in a kindred with phenotypic features of Bartsocas-Papas and CHAND syndromes. Am J Med Genet A. 2015 Nov; 167A(11):2555-62.
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Identification of an Alu-mediated 12.2-kb deletion of the complete LPAR6 (P2RY5) gene in a Turkish family with hypotrichosis and woolly hair. Exp Dermatol. 2012 Jun; 21(6):469-71.
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Unveiling the roots of monogenic genodermatoses: genotrichoses as a paradigm. J Invest Dermatol. 2012 Mar; 132(3 Pt 2):906-14.
MeSH information
