Ichthyosis

"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.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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	Ichthyosis Ichthyosis Ichthyoses Xeroderma Xeroderma Xerodermas

Below are MeSH descriptors whose meaning is more general than "Ichthyosis".

Diseases [C]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Skin Abnormalities [C16.131.831]
Ichthyosis [C16.131.831.512]
Infant, Newborn, Diseases [C16.614]
Ichthyosis [C16.614.492]
Skin and Connective Tissue Diseases [C17]
Skin Diseases [C17.800]
Keratosis [C17.800.428]
Ichthyosis [C17.800.428.333]
Skin Abnormalities [C17.800.804]
Ichthyosis [C17.800.804.512]

Below are MeSH descriptors whose meaning is related to "Ichthyosis".

Below are MeSH descriptors whose meaning is more specific than "Ichthyosis".

publications

Timeline | Most Recent

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.

Bar chart showing 6 publications over 5 distinct years, with a maximum of 2 publications in 2008

To see the data from this visualization as text, click here.

Year	Major Topic	Total
2003	1	1
2008	2	2
2012	1	1
2020	1	1
2024	1	1

Below are the most recent publications written about "Ichthyosis" by people in Profiles.

Ho M, Nguyen HN, Van Hoang M, Bui TTT, Vu BQ, Dinh THT, Vo HTM, Blaydon DC, Eldirany SA, Bunick CG, Bui CB. Altered skin microbiome, inflammation, and JAK/STAT signaling in Southeast Asian ichthyosis patients. Hum Genomics. 2024 04 16; 18(1):38.

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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.

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