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具有独特面容、新生儿肌张力减退、智力障碍和牙齿发育不全的类Ohdo睑裂狭小综合征

Ohdo-like blepharophimosis syndrome with distinctive facies, neonatal hypotonia, mental retardation and hypoplastic teeth.

作者信息

Clayton-Smith J, Krajewska-Walasek M, Fryer A, Donnai D

机构信息

Regional Genetics Service, St Mary's Hospital, Manchester, UK.

出版信息

Clin Dysmorphol. 1994 Apr;3(2):115-20.

PMID:8055130
Abstract

We report four children with unusual facial features including severe blepharophimosis, ptosis, and a distinctive nose with a broad flat tip and a depressed bridge. All four patients were markedly hypotonic and had severe feeding difficulties and developmental delay. Two had congenital heart defects and all three who survived had hypoplastic teeth. Both of the male patients had cryptorchidism. These four children have a distinctive syndrome which is similar to that reported by Biesecker (J Med Genet (1991) 28: 131-134).

摘要

我们报告了4名面部特征异常的儿童,包括严重的睑裂狭小、上睑下垂,以及独特的鼻子,鼻尖宽阔扁平且鼻梁凹陷。所有4例患者均明显肌张力减退,存在严重的喂养困难和发育迟缓。2例有先天性心脏缺陷,存活的3例均有牙齿发育不全。2例男性患者均有隐睾症。这4名儿童患有一种独特的综合征,与Biesecker报告的综合征相似(《医学遗传学杂志》(1991年)28卷:131 - 134页)。

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