Acrokeratosis Verruciformis (Hopf) and Darier's Disease
- 1 March 1966
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of Dermatology
- Vol. 93 (3) , 305-310
- https://doi.org/10.1001/archderm.1966.01600210041006
Abstract
Twelve members of a single family were found to exhibit a disorder of keratinization. Seven of these persons had findings characteristic of Ackrokeratosis Verruciformis (Hopf), one member or possibly two had Darier's disease, and three of the family had minor disturbances of keratinization. It was proposed that these disorders represent variable manifestations of a single underlying genetic defect in keratin formation.This publication has 5 references indexed in Scilit:
- An Electron-Microscope Study of Dyskeratosis and Acantholysis in Darier's Disease**From the Department of PathologyThis study was supported by Grants C-4955, GM-9726, and 2A-5220 (C-1) from the National Institutes of Health, United States Public Health service.Journal of Investigative Dermatology, 1963
- VESICULAR DARIER'S DISEASE (SO-CALLED BENIGN FAMILIAL PEMPHIGUS)Archives of Dermatology and Syphilology, 1950
- CHRONIC BENIGN FAMILIAL PEMPHIGUS, A PROBABLE VESICULAR VARIANT OF KERATOSIS FOLLICULARISArchives of Dermatology, 1950
- HYPERTROPHIC DARIER'S DISEASE AND NEVUS SYRINGOCYSTADENOMATOSUS PAPILLIFERUSArchives of Dermatology and Syphilology, 1949
- ACROKERATOSIS VERRUCIFORMIS (HOPF)Archives of Dermatology and Syphilology, 1947