Duodenal atresia with apple-peel jujenoilial deformity: Case report and review of the literature

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Duodenal atresia with apple-peel jujenoilial deformity: Case report and review of the literature

Duodenal atresia (DA) with small bowel atresia is an extremely rare condition. The widely accepted theory beyond DA development differs from that for small bowel atresia. We report here a case of a baby having both conditions. 2014 The Authors. Published by Elsevier Inc. All rights reserved. Duodenal atresia is believed to occur due to failure of recanalization, whereas jejunal atresia is due t...

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Duodenal Atresia Associated with Apple Peel Atresia and Situs Inversus Abdominus: A Case Report

Duodenal atresia is rarely associated with situs inversus abdominus. We report a case of duodenal atresia associated with small bowel atresia of apple peel type and situs inversus abdominus.

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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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Duodenal atresia with apple-peel configuration of the ileum and absent superior mesenteric artery

BACKGROUND Embryologically, duodenal atresia results from inadequate recanalisation and proliferation of gut epithelius in the 6th week of gestation, while apple-pee atresia of small bowel is a consequence of a vascular accident in subsequent embryonic development, and the two are rather rarely manifested as a joint clinical entity. CASE PRESENTATION We present here a 29 week preterm boy admi...

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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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ژورنال

عنوان ژورنال: Journal of Pediatric Surgery Case Reports

سال: 2014

ISSN: 2213-5766

DOI: 10.1016/j.epsc.2014.03.001