Fragile X-associated tremor/ataxia syndrome: phenotypic comparisons with other movement disorders.
作者： Erin E. Robertson , Deborah A. Hall , Andrew R. McAsey , Joan A. O’Keefe
DOI: 10.1080/13854046.2016.1202239
关键词: Essential tremor 、 Progressive supranuclear palsy 、 Fragile X syndrome 、 Ataxia 、 Psychology 、 Movement disorders 、 Fragile X-associated tremor/ataxia syndrome 、 Neuroscience 、 Spinocerebellar ataxia 、 Age of onset
摘要: AbstractObjective: The purpose of this paper is to review the typical cognitive and motor impairments seen in fragile X-associated tremor/ataxia syndrome (FXTAS), essential tremor (ET), Parkinson disease (PD), spinocerebellar ataxias (SCAs), multiple system atrophy (MSA), progressive supranuclear palsy (PSP) order enhance diagnosis FXTAS patients. Methods: We compared phenotypes with each these other movement disorders. Relevant neuropathological neuroimaging findings are also reviewed. Finally, we describe differences age onset, severity, progression rates, average lifespan ET, PD, SCAs, MSA, PSP. conclude a flow chart algorithm guide clinician differential FXTAS. Results: By comparing PSP have clarified potential symptom overlap while elucidating factors that make disorders...
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