A very rare cause of diarrhea: epidermolysis bullosa.

نویسندگان

  • Tarık Akar
  • Gökhan Dindar
چکیده

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A newborn presenting with epidermolysis bullosa with duodenal atresia: A very rare case report and review of the literature

Background: Epidermolysis bullosa (EB) comprises a group of genetically determined skin fragility disorders, which are characterized by blistering of the skin and mucosa, in response to little or no apparent trauma. These disorders represent heterogeneous phenotypes and are associated with various complications ranging from localized skin fragility to neonatal death. Nevertheless, the term "Epi...

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Pretibial Epidermolysis Bullosa: Report of two cases

Pretibial epidermolysis bullosa is a rare variant of hereditary epidermolysis bullosa characterized by the delayed onset of lesions and their localization. We present two cases, a 35-year-old woman and a 21-year-old man. They clinically had pruritus, nodular prurigo-like or lichenified lesions, violaceous scarring, milia, nail dystrophy and in one case albopapuloid lesions on the trunk. Physica...

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Epidermolysis bullosa is a rare inherited bullous disease with unknown prevalence in most parts of the world. In Saudi Arabia the reported studies regarding epidermolysis bullosa are very limited. This paper presents the first study of epidermolysis bullosa cases from the Western province of Saudi Arabia. We studied 15 cases of inherited epidermolysis bullosa and classified the cases based on e...

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عنوان ژورنال:
  • The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology

دوره 25 4  شماره 

صفحات  -

تاریخ انتشار 2014