Volume 57, Issue 2 (8 1999)
Tehran Univ Med J 1999, 57(2): 84-87 |
Back to browse issues page
Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:
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: (5193 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
| Rights and permissions | |
 |
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. |
