22q11 deletion and polymicrogyria - cause or coincidence?

被引：26
作者：
Worthington, S
Turner, A
Elber, J
Andrews, PI
机构：
[1] Sydney Childrens Hosp, Dept Med Genet, Sydney, NSW, Australia
[2] St George Hosp, Sydney, NSW, Australia
[3] Univ New S Wales, Sch Paediat, Kensington, NSW 2033, Australia
[4] Sydney Childrens Hosp, Sydney, NSW, Australia
来源：
CLINICAL DYSMORPHOLOGY | 2000年 / 9卷 / 03期
关键词：
cortical development disorder; 22q11; deletion; polymicrogyria; Velocardiofacial syndrome;
D O I：
10.1097/00019605-200009030-00008
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
We report a familial case of velocardiofacial syndrome (VCFS) with polymicrogyria to provide further support for the association of disorders of cortical development with del(22q11) syndromes. Clin Dysmorphol 9: 193-197 (C) 2000 Lippincott Williams & Wilkins.
引用
收藏
页码：193 / 197
页数：5
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