Hereditary Acrokeratotic Poikiloderma
- 1 April 1971
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of Dermatology
- Vol. 103 (4) , 409-422
- https://doi.org/10.1001/archderm.1971.04000160059010
Abstract
A dominantly inherited disorder has affected ten members of a family group. At present we recognize the following categories of clinical involvement: (1) vesicopustule formation which remains confined to the hands and feet (this process commences at from 1 to 3 months of age and resolves in late childhood); (2) widespread eczematous dermatitis somewhat resembling atopic eczema which starts between the ages of 3 and 6 months and completely resolves by 5 years of age; (3) the gradual appearance of a diffuse poikiloderma with striate and reticulate atrophy which spares only the face, scalp, and ears (the poikiloderma persists into adult life); and (4) the development of keratotic papules on the hands, feet, elbows, and knees, which first appear at varying times prior to 5 years of age and persist indefinitely.Keywords
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