Storey Elsdon
Department of Medicine (Neuroscience), Monash University, Alfred Hospital Campus, Commercial Road, Melbourne, VIC, 3004, Australia.
Department of Neuroscience, Alfred Hospital, Commercial Road, Melbourne, VIC, 3004, Australia.
Cerebellum. 2016 Feb;15(1):26-29. doi: 10.1007/s12311-015-0721-5.
While the onset of a dominantly inherited ataxia is typically taken to be the onset of gait ataxia, a wide range of other symptoms related to central and/or peripheral nervous system impairment, or even to non-neurological involvement, can be the presenting feature. Knowledge of these is fairly robust for the commonest spinocerebellar ataxias (SCAs 1, 2, 3 and 6) and for those where a striking non-ataxic presentation is the norm (SCAs 7 and 12), but the literature is potentially misleading in the rarer dominant ataxias. This review summarises what is currently known of these non-ataxic presentations and outlines and explains the difficulties associated with determining non-ataxic presentations of dominant ataxias. The relevant literature was surveyed, including systematic reviews (where available) and case reports. Non-ataxic presentations of dominant ataxias are classified by symptom.
虽然常染色体显性遗传性共济失调的发病通常被认为是步态共济失调的开始,但一系列与中枢和/或外周神经系统损害甚至非神经学累及相关的其他症状也可能是首发特征。对于最常见的脊髓小脑共济失调(SCA1、2、3和6型)以及那些以显著的非共济失调表现为常态的类型(SCA7和12型),人们对这些症状的了解相当充分,但在较罕见的显性共济失调中,相关文献可能会产生误导。本综述总结了目前已知的这些非共济失调表现,并概述和解释了在确定显性共济失调的非共济失调表现时所面临的困难。我们检索了相关文献,包括系统评价(如有)和病例报告。显性共济失调的非共济失调表现按症状进行分类。