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PMID: 23431751 已发表 · ppublish 英语

De novo satellited 2q associated with corpus callosum dysgenesis, short stature, mental retardation and developmental delay.

Genetic counseling (Geneva, Switzerland) ·第 23 卷 ·第 4 期 ·2013-04-04

Chen C-P, Lin S-P, Huang Y-L, Chern S-R, Su J-W, Lee C-C, Chen W-L, Wang W

摘要

We report the cytogenetic and molecular characterization of a 9.46-Mb terminal deletion of 2q in a 3-year-old girl with a de novo satellited 2q (2qs), corpus callosum dysgenesis, short stature, mental retardation and developmental delay. We speculate that haploinsufficiency of HDAC4 is responsible for short stature, mental retardation and developmental delay, and haploinsufficiency of EFHD1 is most likely responsible for the phenotype of corpus callosum dysgenesis in this patient.

文献信息
期刊
Genetic counseling (Geneva, Switzerland)
期刊简称
Genet Couns
发表日期
2013-04-04
收录日期
2013-02-25
更新日期
2013-02-25
语言
英语
国家/地区
Switzerland
NLM ID
9015261
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