SECKEL SYNDROME IN A YEMENI FAMILY IN SAUDI-ARABIA

被引:17
作者
KRISHNA, AG
SCRIMGEOUR, EM
ZAWAWI, TH
机构
[1] Department of Medicine, National Guard King Khalid Hospital, Jeddah 21423
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1994年 / 51卷 / 03期
关键词
MICROCEPHALIC; PRIMORDIAL; DWARFISM; SECKEL SYNDROME; YEMENI ARAB OCCURRENCE; AUTOSOMAL RECESSIVE INHERITANCE;
D O I
10.1002/ajmg.1320510310
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We studied a 28-year-old Yemeni woman with typical Seckel syndrome. Two deceased sibs, a twin sister and a brother, had also been affected. The father of these individuals was married to his cousin's daughter: the pedigree suggests autosomal recessive inheritance. Classical Seckel syndrome has not been reported previously in Arabs, and this appears to be the first report from the Middle East. (C) 1994 Wiley-Liss, Inc.
引用
收藏
页码:224 / 227
页数:4
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