Childhood onset of progressive cerebellar ataxia, dysphagia, loss of mental function, blindness, skin pigment abnormalities, and muscle atrophy; likely disorder of iron storage. Condition is autosomal dominant. Death occurs 10Ð20 years after onset.
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Childhood onset of progressive cerebellar ataxia, dysphagia, loss of mental function, blindness, skin pigment abnormalities, and muscle atrophy; likely disorder of iron storage. Condition is autosomal dominant. Death occurs 10Ð20 years after onset.