Trisomy 15q25.2-qter in an autistic child: Genotype-phenotype correlations

被引:15
|
作者
Bonati, MT
Finelli, P
Giardino, D
Gottardi, G
Roberts, W
Larizza, L
机构
[1] Ist Auxol Italiano, Clin Med Genet, Milan, Italy
[2] Ist Auxol Italiano, Lab Med Cytogenet & Mol Genet, Milan, Italy
[3] Univ Milan, Dept Genet & Biol Med Sci, Milan, Italy
[4] Univ Toronto, Hosp Sick Children, Child Dev Ctr, Toronto, ON M5G 1X8, Canada
关键词
autism; complex neurodevelopmental disorder; duplication; FISH mapping; non homologous end joining; pure trisomy 15q25.2-qter;
D O I
10.1002/ajmg.a.30503
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We report on the case of a male child with autistic disorder, postnatal overgrowth, and a minor brain malformation. Karyotyping and fluorescent in situ hybridization (FISH) analysis showed the presence of an extra copy of the distal portion of chromosome 15q (15q25.2-qter) transposed to chromosome 15p leading to 15q25.2-qter pure trisomy. This karyotype-phenotype study further supports the evidence for a specific phenotype related to trisomy 15q25 or 26-qter and suggests that distal chromosome 15q may be implicated in specific behavioral phenotypes. (C) 2005 Wiley-Liss, Inc.
引用
收藏
页码:184 / 188
页数:5
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