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Epidermólisis ampollosa con atresia pilórica: reporte de dos casos en hermanos consecutivos
Author(s) -
Katherine Márquez,
Diego Andrés Rodríguez,
Luis Pérez,
Maurício Duarte,
Luis Augusto Zárate
Publication year - 2021
Publication title -
biomédica/biomedica
Language(s) - Spanish
Resource type - Journals
SCImago Journal Rank - 0.26
H-Index - 28
eISSN - 2590-7379
pISSN - 0120-4157
DOI - 10.7705/biomedica.5401
Subject(s) - medicine , atresia , epidermolysis bullosa , gynecology , humanities , anatomy , dermatology , philosophy
Pyloric atresia is a rare digestive malformation. It represents about 1% of intestinal atresias and is associated with some other genetic or anatomical alteration in 55% of the cases. In 20% of them, it is associated with epidermolysis bullosa, which is described as an established syndrome with a bad prognosis. We present two cases of consecutive siblings with this condition and fatal outcomes in both of them. We made a review of the literature and discussed the main topics.

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