CLINICAL CASE OF PALMOPLANTAR KERATODERMA TYPE UNNA-THOST
نویسندگان
چکیده
منابع مشابه
Unna-Thost-type palmoplantar keratoderma. A case report.
Unna-Thost keratoderma is an autosomal dominant inherited disorder of keratinization, with mutation in Keratin 1 gene. The eponym refers specifically to nonepidermolytic keratoderma, although the original Thost family is now known to have had epidermolytic keratoderma. The condition usually presents in the first few months of life and is usually obvious by the age of 4 years. It rarely appears ...
متن کاملDiffuse epidermolytic palmoplantar keratoderma (Unna-Thost-).
DESCRIPTION We report the case of a 28-year-old man presenting to our hospital with refractory diffuse hyperkeratosis of palms and soles. He reported first appearance in early childhood. His first-born daughter also developed hyperkeratosis on palms and soles directly after birth. No other family member seems to be affected by similar skin lesions. Clinically, our patient presented diffuse hype...
متن کاملWatcher’s type of palmoplantar keratoderma
A 51-year-old man reported with progressive thickening of the skin of the hands and feet since the age of 6yrs. It was largely asymptoma c; however, brisk walking caused excessive swea ng, pain, and widening of the fissures on the soles of the feet. He also had scaly raised lesions on legs and knees. His mother, maternal aunt, cousin and nephew had similar lesions. Examination of the soles of f...
متن کاملBrunauer-Fuhs-Siemens palmoplantar keratoderma: A rare, striate type of focal palmoplantar keratoderma
Brunauer-Fuhs-Siemens palmoplantar keratoderma, commonly known as striate palmoplantar keratoderma, is a rare, autosomally inherited disease of linear hyperkeratosis in which patient usually presents with conspicuous longitudinal hyperkeratosis on volar surface of hands and feet. Mutations in 3 genes namely desmoglein 1, desmoplakin and keratin 1, have been identified and held responsible for t...
متن کاملHereditary palmoplantar keratoderma type papulosa in Slovenia.
BACKGROUND Hereditary palmoplantar keratodermas (HPPK) are relatively frequent in Slovenia; however, the papulosa type of HPPK is rare. Epidemiological data are scarce; a population study in Croatia revealed a prevalence of 1.17/100,000 inhabitants. According to the preliminary data, it seems that HPPK papulosa is more common in Slovenia than in other countries. Efforts were made to identify al...
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ژورنال
عنوان ژورنال: Russian Journal of Skin and Venereal Diseases
سال: 2017
ISSN: 2412-9097,1560-9588
DOI: 10.18821/1560-9588-2017-20-3-143-145