脑源性黄瘤病
医学
共济失调
白内障
儿科
神经退行性变
内科学
精神科
疾病
眼科
胆固醇
作者
Seyed Mohammad Baghbanian,Mohammad Reza Mahdavi,Hadi Majidi
标识
DOI:10.1136/practneurol-2020-002895
摘要
Cerebrotendinous xanthomatosis is a rare autosomal recessive lipid storage syndrome defined clinically by the triad of progressive neurodegeneration, juvenile cataracts and tendon xanthomas in adults. It is treatable, and a prompt diagnosis can improve outcomes. We describe a patient with this condition who presented with progressive ataxia.
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