THE OHDO BLEPHAROPHIMOSIS SYNDROME - A 3RD CASE

被引：25

作者：

BIESECKER, LG

机构：

[1] Department of Pediatrics, University of Michigan, Medical Center, Ann Arbor, MI 48109-0718

来源：

JOURNAL OF MEDICAL GENETICS | 1991年 / 28卷 / 02期

关键词：

D O I：

10.1136/jmg.28.2.131

中图分类号：

Q3 [遗传学];

学科分类号：

071007 [遗传学]; 090102 [作物遗传育种];

摘要：

A patient with a syndrome consisting of blepharophimosis, simple ears, hypoplastic teeth, developmental delay, and hypotonia is described. Previous case reports are reviewed and a differential diagnosis is described. Many of the features in the subject are similar to those described in two previous reports and they constitute a distinct syndrome.

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页码：131 / 134

页数：4

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