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沙赫-瓦登伯格综合征

Shah-Waardenburg syndrome.

作者信息

Mahmoudi Abdelhalim, Rami Mohamed, Khattala Khalid, Elmadi Aziz, Afifi My Abderrahmane, Youssef Bouabdallah

机构信息

Department of Pediatric Surgery, University Hospital Hassan II, Fez, Morocco.

出版信息

Pan Afr Med J. 2013;14:60. doi: 10.11604/pamj.2013.14.60.1543. Epub 2013 Feb 12.

Abstract

Shah-Waardenburg syndrome (SWS) is a neurocristopathy and is characterized by Hirschsprung's disease (HD), deafness, and depigmentation of hairs, skin, and iris. Is a very rare congenital disorder with variable clinical expression. This report describes a 4-day-old male newborn with Waardenburg's syndrome associated with aganglionosis of the colon and terminal ileum, and review the relevant literature for draws attention to the causal relationship between these two entities.

摘要

沙阿-瓦登伯格综合征(SWS)是一种神经嵴病,其特征为先天性巨结肠(HD)、耳聋以及毛发、皮肤和虹膜色素脱失。它是一种临床表型多样的非常罕见的先天性疾病。本报告描述了一名患有瓦登伯格综合征并伴有结肠和回肠末端神经节细胞缺乏症的4日龄男婴,并回顾相关文献以引起对这两种疾病因果关系的关注。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba33/3617621/c1feb703d61f/PAMJ-14-60-g001.jpg

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