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FBN1错义突变的纯合性:隐性马凡综合征的临床和分子证据。

Homozygosity for a FBN1 missense mutation: clinical and molecular evidence for recessive Marfan syndrome.

作者信息

de Vries Bert B A, Pals Gerard, Odink Roelof, Hamel Ben C J

机构信息

Department of Human Genetics, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.

出版信息

Eur J Hum Genet. 2007 Sep;15(9):930-5. doi: 10.1038/sj.ejhg.5201865. Epub 2007 Jun 13.

Abstract

Marfan syndrome (MFS) is known as an autosomal-dominant connective tissue disorder (MIM 154,700), involving primarily the skeletal, ocular and cardiovascular systems, and caused by mutations in the gene for fibrillin1 (FBN1). Here, we report on two cousins from a consanguineous family with a homozygous c.1,453C>T FBN1 mutation (p.Arg485Cys) and MFS. All four healthy parents were heterozygous for the c.1,453C>T FBN1 mutation and none fulfilled the Ghent criteria for MFS. This family is the first molecularly confirmed recessive MFS. The demonstration of recessive cases of MFS has obvious implications for genetic counselling as well as for molecular diagnosis.

摘要

马凡综合征(MFS)是一种常染色体显性结缔组织疾病(MIM 154,700),主要累及骨骼、眼部和心血管系统,由原纤蛋白1(FBN1)基因突变引起。在此,我们报告了来自一个近亲家庭的两名表亲,他们患有纯合子c.1,453C>T FBN1突变(p.Arg485Cys)和马凡综合征。所有四位健康的父母均为c.1,453C>T FBN1突变的杂合子,且均不符合马凡综合征的根特标准。这个家族是首例经分子学证实的隐性马凡综合征。隐性马凡综合征病例的证实对遗传咨询以及分子诊断具有明显意义。

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