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遗传性运动感觉神经病。夏科-马里-图思综合征。

Hereditary motor-sensory neuropathies. Charcot-Marie-Tooth syndrome.

作者信息

Bird T D

机构信息

VA Medical Center, University of Washington Medical School, Seattle.

出版信息

Neurol Clin. 1989 Feb;7(1):9-23.

PMID:2646524
Abstract

The Charcot-Marie-Tooth (CMT) syndrome is also referred to as hereditary motor-sensory neuropathy (HMSN). It is not a single disease but has a multitude of genetic causes. The typical clinical characteristics are distal muscle weakness and atrophy, depressed tendon reflexes, often slow motor NCV, and the frequent finding of other similarly affected relatives. The most common variant of this syndrome is HMSN-I showing autosomal dominant inheritance, markedly slow motor NCV and nerve hypertrophy. One form of HMSN-I is linked to the Duffy locus on chromosome 1. There are numerous other varieties of HMSN including other autosomal dominant conditions such as HMSN-II (with nearly normal motor NCV) and several types of familial amyloid neuropathy (with specific amino acid substitutions in transthyretin); autosomal recessive conditions such as HMSN-III (Déjérine-Sottas hypertrophic neuropathy of childhood) and Refsum's disease (defect of phytanic acid metabolism); and conditions produced by mutations on the X chromosome such as X-linked HMSN, Fabry trihexoside storage disease, and adrenomyeloneuropathy. The known biochemical abnormalities, chromosomal locations, clinical findings and genetic counseling of these disorders are reviewed.

摘要

夏科-马里-图思(CMT)综合征也被称为遗传性运动感觉神经病(HMSN)。它并非单一疾病,而是有多种遗传病因。典型的临床特征包括远端肌肉无力和萎缩、腱反射减弱、运动神经传导速度(NCV)通常减慢,以及经常发现其他有类似症状的亲属。该综合征最常见的变异型是HMSN-I,呈常染色体显性遗传,运动NCV明显减慢且神经肥大。HMSN-I的一种形式与1号染色体上的达菲位点相关。还有许多其他类型的HMSN,包括其他常染色体显性疾病,如HMSN-II(运动NCV近乎正常)和几种家族性淀粉样神经病(转甲状腺素蛋白中有特定氨基酸替代);常染色体隐性疾病,如HMSN-III(儿童期Déjérine-Sottas肥厚性神经病)和Refsum病(植烷酸代谢缺陷);以及由X染色体突变引起的疾病,如X连锁HMSN、法布里三己糖贮积病和肾上腺脊髓神经病。本文对这些疾病已知的生化异常、染色体定位、临床发现和遗传咨询进行了综述。

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