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与眼部和肢体远端缺陷相关的颅缝早闭很可能是由不同于FGFR、TWIST和MSX2的基因中的突变引起的。

Craniosynostosis associated with ocular and distal limb defects is very likely caused by mutations in a gene different from FGFR, TWIST, and MSX2.

作者信息

Passos-Bueno Maria Rita, Armelin Lucia Maria, Alonso Luís Garcia, Neustein Isaac, Sertié Andréa L, Abe Kikue, Pavanello Rita de Cássia, Elkis Lívia C, Koiffmann Célia P

机构信息

Centro de Estudo do Genoma Humano, Departamento de Biologia, Instituto de Biociências, Universidade de São Paulo, São Paulo, Brazil.

出版信息

Am J Med Genet. 2002 Nov 22;113(2):200-6. doi: 10.1002/ajmg.10752.

Abstract

Craniosynostosis caused by genetic factors includes a heterogeneous group of over 100 syndromes, most with autosomal dominant inheritance. Mutations in five genes (FGFR1-, -2, -3, TWIST, and MSX2) causing craniosynostosis as the main clinical feature were described. In most of these conditions, there are also limb malformations. We report a two-generation kindred segregating microcornea, optic nerve alterations and cataract since childhood, craniosynostosis, and distal limb alterations, with a great clinical intrafamilial variability. The ophthalmological problems here described seem to be unique to this genealogy while similar feet alterations were apparently only described in two other affected siblings with acro-cranial-facial dysostosis syndrome (ADS). However, ADS has an autosomal recessive inheritance instead of the dominant pattern of the present genealogy. The candidate exons of the five genes previously mentioned were tested through sequencing analysis presenting normal results in all cases. Therefore, clinical and laboratory analyses in our patients suggest that their phenotype represents a new syndrome very likely caused by mutation in a gene different from those studied.

摘要

由遗传因素引起的颅缝早闭包括100多种不同的综合征,大多数为常染色体显性遗传。已描述了五个基因(FGFR1、-2、-3、TWIST和MSX2)的突变,这些突变以颅缝早闭为主要临床特征。在大多数这些病症中,还存在肢体畸形。我们报告了一个两代家族,自儿童期起就分离出小角膜、视神经改变和白内障、颅缝早闭以及远端肢体改变,家族内临床变异性很大。这里描述的眼科问题似乎是这个家系所特有的,而类似的足部改变显然仅在另外两名患有肢颅面骨发育不全综合征(ADS)的患病兄弟姐妹中被描述过。然而,ADS是常染色体隐性遗传,而非本家系的显性遗传模式。通过测序分析对上述五个基因的候选外显子进行了检测,所有病例结果均正常。因此,对我们患者的临床和实验室分析表明,他们的表型代表一种很可能由不同于所研究基因的基因突变引起的新综合征。

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