"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
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| 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 |
|---|
| 1996 | 1 | 0 | 1 |
| 2012 | 1 | 1 | 2 |
| 2018 | 0 | 1 | 1 |
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Below are the most recent publications written about "Ichthyosis" by people in Profiles.
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In-person validation of the Ichthyosis Scoring System. Pediatr Dermatol. 2024 Mar-Apr; 41(2):247-252.
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Consensus recommendations for the use of retinoids in ichthyosis and other disorders of cornification in children and adolescents. Pediatr Dermatol. 2021 Jan; 38(1):164-180.
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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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Primary cutaneous follicle center lymphoma mimicking folliculitis. Cutis. 2018 Jan; 101(1):E30-E33.
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Meibomian gland dysfunction in a case of ichthyosis follicularis with alopecia and photophobia syndrome. Indian J Ophthalmol. 2014 Mar; 62(3):365-7.
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Complications of ichthyosis beyond the skin. Dermatol Ther. 2013 Jan-Feb; 26(1):39-45.
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A spontaneous Fatp4/Scl27a4 splice site mutation in a new murine model for congenital ichthyosis. PLoS One. 2012; 7(11):e50634.
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Identification of a novel mutation in ZAP70 and prenatal diagnosis in a Turkish family with severe combined immunodeficiency disorder. Gene. 2013 Jan 10; 512(2):189-93.
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Ichthyosiform sarcoidosis: A case report and review of the literature. Dermatol Online J. 2010 Aug 15; 16(8):5.
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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.