"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
|
| Concept/Terms |
|
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 |
|---|
| 1997 | 1 | 0 | 1 |
| 2018 | 0 | 1 | 1 |
| 2020 | 1 | 0 | 1 |
| 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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Hashitoxicosis in a patient with Nicolaides-Baraitser Syndrome: a case report. Clin Dysmorphol. 2023 04 01; 32(2):77-79.
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De novo SMARCA2 variants clustered outside the helicase domain cause a new recognizable syndrome with intellectual disability and blepharophimosis distinct from Nicolaides-Baraitser syndrome. Genet Med. 2020 11; 22(11):1838-1850.
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BAFopathies' DNA methylation epi-signatures demonstrate diagnostic utility and functional continuum of Coffin-Siris and Nicolaides-Baraitser syndromes. Nat Commun. 2018 11 20; 9(1):4885.
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A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family. Eur J Dermatol. 2018 Apr 01; 28(2):209-216.
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A Comprehensive Approach to Multimodal Facial Aesthetic Treatment: Injection Techniques and Treatment Characteristics From the HARMONY Study. Dermatol Surg. 2016 May; 42 Suppl 2:S177-91.
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A recurrent intragenic deletion mutation in DSG4 gene in three Pakistani families with autosomal recessive hypotrichosis. J Invest Dermatol. 2004 Jul; 123(1):247-8.
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A locus for hereditary hypotrichosis localized to human chromosome 18q21.1. Eur J Hum Genet. 2003 Aug; 11(8):623-8.
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Homozygosity mapping of a locus for a novel syndromic ichthyosis to chromosome 3q27-q28. J Invest Dermatol. 2002 Jul; 119(1):70-6.
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Sch?pf-Schulz-Passarge syndrome with an unusual pattern of inheritance. Am J Med Genet. 1997 Aug 08; 71(2):186-8.