"Hypotrichosis" 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.
Presence of less than the normal amount of hair. (Dorland, 27th ed)
Descriptor ID |
D007039
|
MeSH Number(s) |
C17.800.329.937
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Hypotrichosis".
Below are MeSH descriptors whose meaning is more specific than "Hypotrichosis".
This graph shows the total number of publications written about "Hypotrichosis" by people in this website by year, and whether "Hypotrichosis" 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 |
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2000 | 1 | 0 | 1 |
2003 | 1 | 0 | 1 |
2008 | 2 | 0 | 2 |
2009 | 4 | 0 | 4 |
2010 | 1 | 2 | 3 |
2012 | 5 | 0 | 5 |
2013 | 2 | 0 | 2 |
2014 | 1 | 0 | 1 |
2015 | 1 | 0 | 1 |
2018 | 0 | 1 | 1 |
2019 | 2 | 1 | 3 |
2020 | 1 | 0 | 1 |
2021 | 2 | 0 | 2 |
2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "Hypotrichosis" by people in Profiles.
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Identification of a novel sporadic U2HR pathogenic variant in a patient with Marie Unna hereditary hypotrichosis. Pediatr Dermatol. 2023 May-Jun; 40(3):466-467.
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Four hypotrichosis families with mutations in the gene LSS presenting with and without neurodevelopmental phenotypes. Am J Med Genet A. 2021 12; 185(12):3900-3904.
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Additional causal SNRPE mutations in hereditary hypotrichosis simplex. Br J Dermatol. 2021 08; 185(2):439-441.
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Loss-of-function variants in C3ORF52 result in localized autosomal recessive hypotrichosis. Genet Med. 2020 07; 22(7):1227-1234.
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Autosomal-dominant hypotrichosis with woolly hair: Novel gene locus on chromosome 4q35.1-q35.2. PLoS One. 2019; 14(12):e0225943.
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Two females with hair loss. J Dtsch Dermatol Ges. 2019 08; 17(8):845-847.
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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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Exome sequencing unravels unexpected differential diagnoses in individuals with the tentative diagnosis of Coffin-Siris and Nicolaides-Baraitser syndromes. Hum Genet. 2015 Jun; 134(6):553-68.
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Odd-looking hair and progressive alopecia in mother and son. JAMA Dermatol. 2014 May; 150(5):567-8.