Friedreich Ataxia: current status and future prospects.

Q3 Medicine Cerebellum and Ataxias Pub Date : 2017-04-07 eCollection Date: 2017-01-01 DOI:10.1186/s40673-017-0062-x
Katrin Bürk
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引用次数: 116

Abstract

Friedreich ataxia (FA) represents the most frequent type of inherited ataxia. Most patients carry homozygous GAA expansions in the first intron of the frataxin gene on chromosome 9. Due to epigenetic alterations, frataxin expression is significantly reduced. Frataxin is a mitochondrial protein. Its deficiency leads to mitochondrial iron overload, defective energy supply and generation of reactive oxygen species. This review gives an overview over clinical and genetic aspects of FA and discusses current concepts of frataxin biogenesis and function as well as new therapeutic strategies.

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弗里德赖希共济失调:现状及未来展望。
弗里德赖希共济失调(FA)是最常见的遗传性共济失调类型。大多数患者在9号染色体上fraataxin基因的第一个内含子上携带纯合子GAA扩增。由于表观遗传改变,frataxin的表达显著降低。卵黄蛋白是一种线粒体蛋白。它的缺乏导致线粒体铁超载,能量供应缺陷和活性氧的产生。本文综述了FA的临床和遗传学方面,并讨论了目前关于fraataxin生物发生和功能的概念以及新的治疗策略。
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Cerebellum and Ataxias
Cerebellum and Ataxias Medicine-Neurology (clinical)
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