Mild developmental delay in terminal chromosome 6p deletion

被引:14
作者
Chen, KM
Cherry, AM
Hahn, JS
Enns, GM
机构
[1] Stanford Univ, Med Ctr, Div Med Genet, Dept Pediat,Sch Med, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Pathol, Stanford, CA USA
[3] Stanford Univ, Sch Med, Dept Neurol, Stanford, CA USA
关键词
chromosome 6p deletion; hypertelorism; eye abnormalities; deafness; developmental delay;
D O I
10.1002/ajmg.a.30127
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Deletions involving the short arm of chromosome 6 are relatively rare. Although features of this condition are variable, common findings include developmental delay, ocular abnormalities, hearing loss, and cardiac defects. In an effort to define further the clinical variability of this condition, we report a 6-year-old female with a de novo terminal deletion of chromosome 6 at band 6p24, with mild gross motor delays and normal cognition. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:201 / 205
页数:5
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