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Late onset gait abnormalities associated with MRI documented vermis atrophy have been reported in a single autosomal dominant pedigree. The diagnosis of CFEOM1 was confirmed with molecular studies but only two older individuals aged 79 and 53 years had the cerebellar atrophy while a 33 year old in the same family had only CFEOM with no gait difficulties and no neuroimaging abnormalities.
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