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A Chinese case of fragile X-associated tremor/ataxia syndrome (FXTAS) with orthostatic tremor:case report and literature review on tremor in FXTAS

机译:中国易碎的X相关震颤/ ataxia综合征(Fxtas)的案例:案例报告和FXTAS震颤的文献综述

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Fragile X-associated tremor/ataxia syndrome (FXTAS) is a late onset, X-linked genetic, neurodegenerative disorder caused by a “premutation (PM)” in the fragile X mental retardation 1 (FMR1) gene. Here we report a case of FXTAS from mainland of China who presented with rare orthostatic tremor. A review of tremor of FXTAS in the literature is also included. A 67-year-old right-handed farmer started with tremor of both legs 8?years ago which was present while standing but absent when sitting or lying and progressed with unsteady gait one and a half years ago. The brain MRI showed high intensity signal in the bilateral middle cerebellar peduncles (MCP) in T2-weighted and fluid-attenuated inversion recovery (FLAIR) images and gene test for premutation for FMR1 was positive with 101 CGG repeats. The patient met the the diagnosis of definite FXTAS. Clonazepam and topiramate were administered to control tremor. We reviewed the literature and identified 64 cases with detailed clinical and genetic information. Orthostatic tremor associated with FXTAS is very rare. We found 85.2% patients reported tremor,42.6% with intention tremor,36.1% with kinetic tremor,32.8% with rest tremor and 29.5% with posture tremor. 37.7% of patients who have tremor showed at least two types of tremor. There were 6 patients with isolated rest tremor. There was 2 patient with voice tremor and 6 with head tremor. We also found that 74.6% FXTAS patients had family history of FMR1 gene associated diseases including Fragile X syndrome (FXS), FXTAS or fragile X-associated primary ovarian insufficiency (FXPOI). Adding our data to the available literature suggests that orthostatic tremor could be a rare initial manifestation of FXTAS and the review will increasing our understanding the phenotype of tremor in FXTAS. Family history of FMR1 gene associated diseases might be an important clue to the diagnosis.
机译:脆弱的X相关的震颤/共济失调综合征(FXTAS)是脆弱X心理延迟1(FMR1)基因的“优化(PM)”引起的晚期发作,X-Linked遗传,神经变性障碍。在这里,我们举报了来自中国大陆的FXTAS案例,他们呈现出罕见的直脱石震颤。还包括文献中FXTAS震颤的审查。一名67岁的右手农民从两条腿8的震颤开始?几年前,当时坐着或撒谎时缺席并在一年半前的步态上进展。脑MRI在T2加权和流体衰减的反转恢复(FLAIR)图像中的双侧中部小脑饲养(MCP)中的高强度信号显示,并且对于FMR1的除去的基因测试是阳性的101 CGG重复。患者达到了明确的FXTAS的诊断。克隆泮和托吡酯被施用于控制震颤。我们审查了文献,并确定了64例临床和遗传信息。与FXTAS相关的原角震颤非常罕见。我们发现85.2%的患者报告震颤,有意震颤的42.6%,动态震颤36.1%,32.8%,休息震颤,震颤姿势震颤29.5%。 37.7%的震颤的患者显示至少两种类型的震颤。有6名患者孤立的休息震颤。有2例患者具有语音震颤和6头震颤。我们还发现74.6%的FXTAS患者具有FMR1基因相关疾病的家族史,包括脆弱的X综合征(FXS),FXTAS或脆弱的X相关原发卵巢功能不全(FXPOI)。将我们的数据添加到可用文献中,表明,原位震颤可能是FXTAS的罕见初始表现,审查将增加我们理解FXTAS中震颤的表型。 FMR1基因相关疾病的家族史可能是诊断的重要线索。

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