"Monilethrix" 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.
Rare autosomal dominant disorder of the hair shaft. The clinical features of the disease include HYPOTRICHOSIS, dry, and/or brittle hair, with varying degrees of ALOPECIA. Mutations in the hair-specific keratin genes KRTHB1, KRTHB3, or KRTHB6 are associated with monilethrix. Autosomal recessive monilethrix with limited HYPOTRICHOSIS are also known. Mutations in Dsg4, Liph, and P2ry5 protein genes are associated with the recessive form of monilethrix.
| Descriptor ID |
D056734
|
| MeSH Number(s) |
C16.131.077.592 C16.320.850.647 C17.800.329.984 C17.800.827.602
|
| Concept/Terms |
Monilethrix- Monilethrix
- Monilethrices
- Nodose Hair
- Hair, Nodose
- Hairs, Nodose
- Nodose Hairs
|
Below are MeSH descriptors whose meaning is more general than "Monilethrix".
Below are MeSH descriptors whose meaning is more specific than "Monilethrix".
This graph shows the total number of publications written about "Monilethrix" by people in this website by year, and whether "Monilethrix" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2015 | 1 | 0 | 1 |
| 2017 | 1 | 0 | 1 |
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Below are the most recent publications written about "Monilethrix" by people in Profiles.
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[Monilethrix is a hereditary hair shaft disorder]. Ugeskr Laeger. 2017 Sep 11; 179(37).
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A novel KRT86 mutation in a Turkish family with monilethrix, and identification of maternal mosaicism. Clin Exp Dermatol. 2015 Oct; 40(7):781-5.
MeSH information
