Volume 57, Issue 2 (8 1999)
Tehran Univ Med J 1999, 57(2): 84-87 |
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Seirafi H, Farnaghi F, Daneshpazhooh M. Three familial cases of Pasini variant of dominant dystrophic epidermolysis. Tehran Univ Med J 1999; 57 (2) :84-87
URL: http://tumj.tums.ac.ir/article-1-1479-en.html
URL: http://tumj.tums.ac.ir/article-1-1479-en.html
Abstract: (5143 Views)
Epidermolysis bullosa (EB) is the term applied to a group of disorders whose common primary feature is the formation of blisters following trivial trauma. Hereditary EB comprises 3 major classes: simplex, junctional and dystrophic, and includes more than 23 phenotypes. The albopapuloid pasini variant of dominant dystrophic EB is characterized by a distinctive clinical appearance. In this article, we report this disease in three members of a family (father and two sons).
Keywords: Dystrophic epidermolysis bullosa, Albopapuloid pasini variant of dominant dystrophic epidermolysis bullosa
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