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[遗传性运动和感觉神经病伴近端优势受累(HMSN-P)由TFG基因突变引起]

[Hereditary motor and sensory neuropathy with proximal dominant involvement (HMSN-P) is caused by a mutation in TFG].

作者信息

Ishiura Hiroyuki, Tsuji Shoji

机构信息

Department of Neurology, The University of Tokyo.

出版信息

Rinsho Shinkeigaku. 2013;23(11):1203-5. doi: 10.5692/clinicalneurol.53.1203.

Abstract

Hereditary motor and sensory neuropathy with proximal dominant involvement (HMSN-P) is an autosomal dominant neurodegenerative disease characterized by proximal predominant weakness and muscle atrophy accompanied by distal sensory disturbance. Linkage analysis using 4 families identified a region on chromosome 3 showing a LOD score exceeding 4. Further refinement of candidate region was performed by haplotype analysis using high-density SNP data, resulting in a minimum candidate region spanning 3.3 Mb. Exome analysis of an HMSN-P patient revealed a mutation (c.854C>T, p.Pro285Leu) in TRK-fused gene (TFG). The identical mutation was found in the four families, which cosegregated with the disease. The mutation was neither found in Japanese control subjects nor public databases. Detailed haplotype analysis suggested two independent origins of the mutation. These findings indicate that the mutation in TFG causes HMSN-P.

摘要

遗传性近端为主型运动和感觉神经病(HMSN-P)是一种常染色体显性神经退行性疾病,其特征为近端为主的肌无力和肌肉萎缩,并伴有远端感觉障碍。对4个家族进行连锁分析,确定了3号染色体上一个LOD评分超过4的区域。利用高密度单核苷酸多态性(SNP)数据通过单倍型分析对候选区域进行进一步细化,最终确定了一个最小候选区域,跨度为3.3兆碱基对(Mb)。对一名HMSN-P患者进行外显子组分析,发现TRK融合基因(TFG)存在一个突变(c.854C>T,p.Pro285Leu)。在这4个家族中均发现了相同的突变,且该突变与疾病共分离。在日本对照人群和公共数据库中均未发现该突变。详细的单倍型分析表明该突变有两个独立的起源。这些发现表明TFG中的突变导致了HMSN-P。

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