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Related to ichthyosis vulgaris: atopic dermatitis


A congenital skin disease characterized by dryness and scales, especially on the extensor surfaces of the extremities.
McGraw-Hill Dictionary of Scientific & Technical Terms, 6E, Copyright © 2003 by The McGraw-Hill Companies, Inc.
The following article is from The Great Soviet Encyclopedia (1979). It might be outdated or ideologically biased.



fish skin disease, xeroderma, a skin disease characterized by sharply increased keratogenesis and retarded keratolysis.

Incidence of ichthyosis is a familial condition in half the cases and hereditary in 25 percent. It appears in early childhood (most often around age three), intensifies at puberty, and lasts throughout life. It is expressed in dryness of the skin and the accumulation of horny masses on the skin’s surface, in the form of scales or of massive horny plates that resemble fish scales. The excretion of oil and perspiration decreases sharply. The affection spreads over the entire skin surface, except at joint folds, axillae, and inguinal folds. On the face and scalp, ichthyosis appears in the form of furfuraceous desquamation. The condition of the skin improves in the summertime as a result of increased excretion of oil and sweat. Ichthyosis is treated with hot baths containing soda or table salt, followed by lubrication of the skin with emollient creams. Cod-liver oil and vitamins may be taken internally (in particular vitamin A). In the summer, prolonged sojourns in the south can be helpful (sea bathing).


The Great Soviet Encyclopedia, 3rd Edition (1970-1979). © 2010 The Gale Group, Inc. All rights reserved.
References in periodicals archive ?
Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema.
The earliest insight that filaggrin was clinically important was in 1985, when Sybert and colleagues (13) proposed that it might be associated with the dry scaly skin condition ichthyosis vulgaris. It was only relatively recently, however, that genetic techniques had developed to the point at which it could be demonstrated that loss-of-function mutations in the filaggrin gene cause ichthyosis vulgaris (Figure 1).
It is caused by abnormality in keratinization and exfoliation of the horny cell layer.1 The severity of symptoms can vary enormously, from the mildest types such as ichthyosis vulgaris which may be mistaken for normal dry skin up to life-threatening conditions such as harlequin ichthyosis.
Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris. Nature Genetics, 2006, 38, 337-342.
(8) There may be a familial association with ichthyosis vulgaris and other disorders of keratinization.
A study of 100 amaXhosa children in South Africa with severe AD and ichthyosis vulgaris symptoms revealed no FLG mutations.
Ichthyosis vulgaris. A clinical and histopathological study of patients and their close relatives in the autosomal dominant and sex-linked forms of the disease.
About 18 months ago, the gene was in fact sequenced, and this led to the discovery that mutations in it are linked to ichthyosis vulgaris (in homozygous individuals) and atopic dermatitis (in heterozygotes).