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[脆性X综合征的分子诊断]

[Molecular diagnosis of fragile X syndrome].

作者信息

Ben Jemaa Lamia, Khemir Samah, Maazoul Faouzi, Richard Laurent, Beldjord Cherif, Chaabouni Myriam, Chaabouni Habiba

机构信息

Service des maladies congénitales et héréditaires, EPS Charles Nicolle, Tunis, Tunisie.

出版信息

Tunis Med. 2008 Nov;86(11):973-7.

Abstract

BACKGROUND

The fragile X syndrome was the most frequent etiology of hereditary mental retardation but the clinical diagnosis is not easy and the individual clinical symptoms were not specific so the confirmation will be made par molecular study of the gene of the fragile X syndrome. The aim of our study is to realise the molecular diagnosis of the fragile X syndrome in 200 Tunisian boys with mental retardation. Our results shows that the frequency of the fragile X syndrome is 7,6%. In the most cases there is a family history of mental retardation with medium age at 11 years. All the boys with the full mutation have mental retardation, dysmorphic features and macro-orchidism (pubescent boy)

CONCLUSION

The screening of the molecular abnormalities of FMRI gene must be realised in every boy with mental retardation or boy with delayed speech without any identified etiology. The earlier diagnosis is important for genetic counselling.

摘要

背景

脆性X综合征是遗传性智力障碍最常见的病因,但临床诊断并不容易,且个体临床症状不具特异性,因此需通过对脆性X综合征基因进行分子研究来确诊。我们研究的目的是对200名患有智力障碍的突尼斯男孩进行脆性X综合征的分子诊断。我们的结果显示脆性X综合征的发生率为7.6%。在大多数情况下,有智力障碍家族史,平均年龄为11岁。所有具有完全突变的男孩都有智力障碍、畸形特征和巨睾症(青春期男孩)。

结论

对于每一名患有智力障碍或言语发育迟缓且无明确病因的男孩,都必须进行FMR1基因分子异常的筛查。早期诊断对于遗传咨询很重要。

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