Potocki-Lupski Syndrome: An Inherited dup(17)(p11.2p11.2) With Hypoplastic Left Heart

被引:26
作者
Yusupov, Roman [3 ,4 ]
Roberts, Amy E. [2 ,3 ,4 ]
Lacro, Ronald V. [2 ,3 ]
Sandstrom, Mary [1 ]
Ligon, Azra H. [1 ,3 ]
机构
[1] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
[2] Childrens Hosp, Dept Cardiol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Boston, MA 02115 USA
[4] Childrens Hosp, Div Genet, Boston, MA 02115 USA
关键词
cytogenetic; inherited; duplication; hypoplastic left heart; dup(17)(p11.2p11.2); Potocki-Lupski syndrome; HOMOLOGOUS RECOMBINATION; DUPLICATION; DELETION; CROSSOVERS; MECHANISM;
D O I
10.1002/ajmg.a.33845
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Low copy repeat (LCR) sequences in 17p11.2 predispose this region to genomic deletions and duplications. Duplication of 17p11.2, also known as Potocki-Lupski syndrome (PTLS), is a well-described microduplication syndrome featuring cognitive and language deficits, developmental delay, autistic behavior, structural cardiovascular anomalies, hypotonia, failure to thrive, apnea, and dysmorphism. We present a mother and her two children who share both dysmorphic features and the dup(17) (p11.2p11.2); the first child was born with hypoplastic left heart (HLH). The dup(17)(p11.2p11.2) was identified by GTG-banding analysis of peripheral blood specimens from all three individuals and confirmed by fluorescence in situ hybridization (FISH) and array comparative genomic hybridization (aCGH). Here we provide a thorough description of the phenotypes of the affected individuals, as well as describe physical features not reported previously for PTLS. (C) 2011 Wiley-Liss, Inc.
引用
收藏
页码:367 / 371
页数:5
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