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首例遗传性2q37.3间质性缺失的家族性病例,伴有包括E型短指和身材矮小在内的孤立性骨骼异常。

The first familial case of inherited 2q37.3 interstitial deletion with isolated skeletal abnormalities including brachydactyly type E and short stature.

作者信息

Jean-Marçais Nolwenn, Decamp Matthieu, Gérard Marion, Ribault Virginie, Andrieux Joris, Kottler Marie-Laure, Plessis Ghislaine

机构信息

Service de Génétique, Hôpital Universitaire de la Côte de Nacre, Caen, France; Service de Pédiatrie, Hôpital Universitaire de la Côte de Nacre, Caen, France.

出版信息

Am J Med Genet A. 2015 Jan;167A(1):185-9. doi: 10.1002/ajmg.a.36428. Epub 2014 Nov 17.

Abstract

Albright hereditary osteodystrophy (AHO)-like syndrome is also known as brachydactyly-mental retardation syndrome (BDMR; OMIM 60040). This disorder includes intellectual disability in all patients, skeletal abnormalities, including brachydactyly E (BDE) in approximately half, obesity, and facial dysmorphism. Patients with 2q37 microdeletion or HDAC4 mutation are defined as having an AHO-like phenotype with normal stimulatory G (Gs) function. HDAC4 is involved in neurological, cardiac, and skeletal function. This paper reports the first familial case of 2q37.3 interstitial deletion affecting two genes, HDAC4 and TWIST2. Patients presented with BDE and short stature without intellectual disability, showing that haploinsufficiency of the HDAC4 critical region may lead to a spectrum of phenotypes, ranging from isolated brachydactyly type E to BDMR.

摘要

类奥尔布赖特遗传性骨营养不良(AHO)综合征也称为短指-智力发育迟缓综合征(BDMR;OMIM 60040)。这种疾病在所有患者中都包括智力残疾、骨骼异常,约一半患者有短指E型(BDE)、肥胖和面部畸形。2q37微缺失或HDAC4突变的患者被定义为具有类AHO表型且刺激型G(Gs)功能正常。HDAC4参与神经、心脏和骨骼功能。本文报道了首例影响HDAC4和TWIST2两个基因的2q37.3间质性缺失的家族病例。患者表现为BDE和身材矮小但无智力残疾,表明HDAC4关键区域的单倍剂量不足可能导致一系列表型,从孤立的E型短指到BDMR。

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