"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 |
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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 |
|---|
| 2003 | 1 | 0 | 1 |
| 2008 | 2 | 0 | 2 |
| 2012 | 1 | 0 | 1 |
| 2020 | 1 | 0 | 1 |
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Below are the most recent publications written about "Ichthyosis" by people in Profiles.
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Cave A, Plumptre I, Mellerio JE, Martinez AE, Kinsler VA. The adverse effect profile of acitretin in a pediatric dermatology population-Longitudinal cohort study and recommendations for monitoring. J Am Acad Dermatol. 2020 Dec; 83(6):1779-1781.
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Elaba Z, Hughey L, Isayeva T, Weeks B, Solovan C, Solovastru L, Andea A. Ultrastructural and molecular confirmation of the trichodysplasia spinulosa-associated polyomavirus in biopsies of patients with trichodysplasia spinulosa. J Cutan Pathol. 2012 Nov; 39(11):1004-9.
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Gaines P, Tien CW, Olins AL, Olins DE, Shultz LD, Carney L, Berliner N. Mouse neutrophils lacking lamin B-receptor expression exhibit aberrant development and lack critical functional responses. Exp Hematol. 2008 Aug; 36(8):965-76.
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Zwerger M, Herrmann H, Gaines P, Olins AL, Olins DE. Granulocytic nuclear differentiation of lamin B receptor-deficient mouse EPRO cells. Exp Hematol. 2008 Aug; 36(8):977-87.
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Shultz LD, Lyons BL, Burzenski LM, Gott B, Samuels R, Schweitzer PA, Dreger C, Herrmann H, Kalscheuer V, Olins AL, Olins DE, Sperling K, Hoffmann K. Mutations at the mouse ichthyosis locus are within the lamin B receptor gene: a single gene model for human Pelger-Hu?t anomaly. Hum Mol Genet. 2003 Jan 01; 12(1):61-9.
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Sidransky E, Sherer DM, Ginns EI. Gaucher disease in the neonate: a distinct Gaucher phenotype is analogous to a mouse model created by targeted disruption of the glucocerebrosidase gene. Pediatr Res. 1992 Oct; 32(4):494-8.
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Silvestri DL. Ichthyosiform dermatosis and deafness. Arch Dermatol. 1978 Aug; 114(8):1243-4.
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Green MC, Shultz LD, Nedzi LA. Abnormal nuclear morphology of leukocytes in the mouse mutant ichthyosis. Transplantation. 1975 Aug; 20(2):172-5.