"Ichthyosis" 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.
Any of several generalized skin disorders characterized by dryness, roughness, and scaliness, due to hypertrophy of the stratum corneum epidermis. Most are genetic, but some are acquired, developing in association with other systemic disease or genetic syndrome.
| Descriptor ID |
D007057
|
| MeSH Number(s) |
C16.131.831.512 C16.614.492 C17.800.428.333 C17.800.804.512
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Ichthyosis".
Below are MeSH descriptors whose meaning is more specific than "Ichthyosis".
This graph shows the total number of publications written about "Ichthyosis" by people in this website by year, and whether "Ichthyosis" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2007 | 1 | 0 | 1 |
| 2014 | 1 | 0 | 1 |
| 2018 | 1 | 0 | 1 |
| 2019 | 0 | 1 | 1 |
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Below are the most recent publications written about "Ichthyosis" by people in Profiles.
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Sjogren's syndrome: An update on disease pathogenesis, clinical manifestations and treatment. Clin Immunol. 2019 06; 203:81-121.
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Ichthyosis molecular fingerprinting shows profound TH17 skewing and a unique barrier genomic signature. J Allergy Clin Immunol. 2019 02; 143(2):604-618.
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Activating mutations in STIM1 and ORAI1 cause overlapping syndromes of tubular myopathy and congenital miosis. Proc Natl Acad Sci U S A. 2014 Mar 18; 111(11):4197-202.
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Malignant proliferating pilar tumors arising in KID syndrome: a report of two patients. Am J Med Genet A. 2007 Apr 01; 143A(7):734-41.