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Presence of Middle Cerebellar Peduncle Sign in FMR1 Premutation Carriers Without Tremor and Ataxia

机译:无震颤和共济失调的FMR1突变载体中存在小脑中柄标志

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摘要

Here we report five cases of male FMR1 premutation carriers who present without clinical symptoms of the fragile X-associated tremor/ataxia syndrome (FXTAS), but who on MRI demonstrate white matter hyperintensities in the middle cerebellar peduncles (MCP sign) and other brain regions, a rare finding. MCP sign is the major radiological feature of FXTAS; it is therefore remarkable to identify five cases in which this MRI finding is present in the absence of tremor and ataxia, the major clinical features of FXTAS. Subjects underwent a detailed neurological evaluation, neuropsychological testing, molecular testing, and MRI evaluation utilizing T2 imaging described here. Additional white matter disease was present in the corpus callosum in four of the five cases. However, all cases were asymptomatic for motor signs of FXTAS.
机译:在这里,我们报告了5例男性FMR1突变前携带者,他们没有表现出脆弱的X相关震颤/共济失调综合症(FXTAS)的临床症状,但是在MRI上显示中小脑梗和其他大脑区域的白质过高,这是一个难得的发现。 MCP信号是FXTAS的主要放射学特征;因此,很重要的一点是,确定了5例在没有震颤和共济失调(即FXTAS的主要临床特征)的情况下出现此MRI发现的病例。使用此处描述的T2成像对受试者进行详细的神经学评估,神经心理学测试,分子测试和MRI评估。五例中有四例在call体中存在其他白质病。但是,所有病例均无FXTAS运动症状。

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