Suppr超能文献

一例瓦登伯格综合征合并无神经节症。

A case of Waardenburg syndrome and aganglionosis.

作者信息

Aritürk E, Tosyali N, Aritürk N

机构信息

Department of Pediatric Surgery, Dicle University Faculty of Medicine, Diyarbakir.

出版信息

Turk J Pediatr. 1992 Apr-Jun;34(2):111-4.

PMID:1440950
Abstract

Waardenburg's syndrome is characterized by a broad nasal root, pigmentation disturbance and congenital deafness while aganglionosis is described as the partial or complete lack of ganglion cells in the alimentary tract. This report describes a five-day-old male infant with Waardenburg's syndrome associated with total aganglionosis of the colon, ileum and distal jejunum and draws attention to the causal relationship between these two entities.

摘要

瓦登伯革氏综合征的特征为宽鼻根、色素沉着紊乱和先天性耳聋,而神经节细胞缺乏症是指消化道中部分或完全缺乏神经节细胞。本报告描述了一名患有瓦登伯革氏综合征且伴有结肠、回肠和空肠远端完全性神经节细胞缺乏症的5日龄男婴,并提请注意这两种病症之间的因果关系。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验