The syndrome of hypoparathyroidism, severe growth failure, developmental delay and distinctive facies

被引：12

作者：

AlGazali, LI

Dawodu, A

机构：

[1] Department of Paediatrics, Fac. of Medicine and Health Sciences, United Arab Emirates University, Al Ain

来源：

CLINICAL DYSMORPHOLOGY | 1997年 / 6卷 / 03期

关键词：

hypoparathyroidism; autosomal recessive; Arabs; developmental delay;

D O I：

10.1097/00019605-199707000-00006

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

We report a child from a highly inbred Omani family with hypoparathyroidism, growth failure, developmental delay and a distinctive facial appearance. Thirty cases with this syndrome have been previously reported; 22 came from the Arab Gulf Countries and eight were Arabs living in Israel. These cases are reviewed.

引用

页码：233 / 237

页数：5

共 14 条

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