De novo partial duplication of chromosome 7p in a male with autistic disorder

被引:15
作者
Wolpert, CM
Donnelly, SL
Cuccaro, ML
Hedges, DJ
Poole, CP
Wright, HH
Gilbert, JR
Pericak-Vance, MA
机构
[1] Duke Univ, Med Ctr, Ctr Human Genet, Dept Med, Durham, NC 27710 USA
[2] William S Hall Psychiat Inst, Columbia, SC USA
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 2001年 / 105卷 / 03期
关键词
autistic disorder; partial trisomy 7p; inverted duplication 7p; HOXA1; gene; craniofacial abnormalities;
D O I
10.1002/ajmg.1258
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We describe a de novo partial duplication of 7p in a 25-year-old male with autistic disorder (AD). High-resolution chromosome analysis revealed an extra segment added to the proximal short arm of chromosome 7, The G-band pattern ii;as consistent with an inverted duplication of 7p11.2-p14.1. Fluorescent in situ hybridization (FISH), using a whole chromosome 7 DNA probe (Cytocell, Inc., UR), confirmed that the extra chromosome material is derived from chromosome 7. indicating that the patient is partially trisomic for a region of the short arm of chromosome 7, Partial duplication of the short arm of chromosome 7 is uncommon with little more than 30 eases in the literature. This is the first report of an individual with a 7p duplication who also has AD. (C) 2001 Wiley-Liss, Inc.
引用
收藏
页码:222 / 225
页数:4
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