Update on the Clinical, Radiographic, and Neurobehavioral Manifestations in FXTAS and FMR1 Premutation Carriers.

Update on the Clinical, Radiographic, and Neurobehavioral Manifestations in FXTAS and FMR1 Premutation Carriers.
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DOI:
10.1007/s12311-016-0799-4
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发表时间:
2016-10
期刊:
Cerebellum (London, England)
影响因子:
--
通讯作者:
O'Keefe JA
O'Keefe JA
中科院分区:
其他
文献类型:
--
作者:
Hall DA;Robertson E;Shelton AL;Losh MC;Mila M;Moreno EG;Gomez-Anson B;Martínez-Cerdeño V;Grigsby J;Lozano R;Hagerman R;Maria LS;Berry-Kravis E;O'Keefe JA

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脆性X相关震颤/共济失调综合征(FXTAS)是一种进行性神经退行性疾病,由脆性X智力低下1(FMR 1)基因的重复扩增引起。这种疾病的特征是运动性震颤和小脑共济失调,表现出年龄依赖性震颤,并且更常见于男性。本文总结了FXTAS在2015年第二届FMR 1前突变国际会议上提出的关键新问题:基本机制和临床参与。讨论的主题包括表型-基因型关系,神经行为功能,以及FXTAS遗传学和成像的更新。
Fragile X-associated tremor/ataxia syndrome (FXTAS) is a progressive neurodegenerative disorder caused by a repeat expansion in the fragile X mental retardation 1 (FMR1) gene. The disorder is characterized by kinetic tremor and cerebellar ataxia, shows age-dependent penetrance, and occurs more frequently in men. This paper summarizes the key emerging issues in FXTAS as presented at the Second International Conference on the FMR1 Premutation: Basic Mechanisms & Clinical Involvement in 2015. The topics discussed include phenotype-genotype relationships, neuro-behavioral function, and updates on FXTAS genetics and imaging.
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