Erythrokeratodermia variabilis. A family study.

Erythrokeratodermia variabilis. A family study. Research Abstract Details 

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Erythrokeratodermia variabilis. A family study. Abstract Text:

Erythrokeratodermia variabilis is a rare genodermatosis; American authors have reported only four previous cases. It had been a problem to obtain a large pedigree for clinical investigation. We studied a family with 12 involved members in five generations. Symmetrically distributed migratory patches and scaling plaques are characteristic and were found to involute with a combination of keratolytic agents and topical steroids. Exacerbations of these patches and plaques were noted in our female patients during such high estrogen states as pregnancy or oral contraceptive usage.

Erythrokeratodermia variabilis. A family study. Publishing Authors By Initials

For similar skin and connective tissue diseases: skin diseases research abstracts see: skin and connective tissue diseases: skin diseases research

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Erythrokeratodermia variabilis. A family study. Journal Published:

PUBLICATION TYPE: Journal Article

Journal: Archives of dermatology

VOLUME: 114

Page Numbers: 259-61

Journal Abbreviation: Arch Dermatol

ISSN: 0003-987X

DAY: 17

MONTH: Feb

YEAR: 1978

Erythrokeratodermia variabilis. A family study. Information

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LANGUAGE: eng

NlmUniqueID: 372433

Erythrokeratodermia variabilis. A family study. Keywords Mesh Terms:

KEYWORDS: Skin Diseases

MESH TERMS: pathology

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Country: UNITED STATES

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MEDLINETA: Arch Dermatol

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