The syndrome of hypoparathyroidism, severe growth failure, developmental delay and distinctive facies.
作者信息
al-Gazali L I, Dawodu A
机构信息
Department of Paediatrics, Faculty of Medicine and Health Sciences, United Arab Emirates University, AI Ain, UAE.
出版信息
Clin Dysmorphol. 1997 Jul;6(3):233-7. doi: 10.1097/00019605-199707000-00006.
Abstract
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.
摘要
Zotero 插件