Fahr病:家族性特发性基底神经节钙化伴或不伴锥体外系疾病

A. Castagna, Carmen Ruberto, R. Cerra, L. Greco, G. Ruotolo
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引用次数: 0

摘要

Fahr病(FD),也称为家族性特发性基底节钙化,是一种影响大脑微血管的神经退行性疾病,主要发生在基底节。它主要表现为运动障碍、痴呆和行为异常。它被认为是遗传性的,常染色体显性遗传。Fahr病经常被低估和诊断不足。我们报告了两名Fahr病患者的临床差异。特别是,我们描述了一例Fahr病伴有锥体外系运动障碍的行为改变,以及一例罕见的Fahr病在没有锥体外系活动障碍的情况下伴有认知和行为改变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fahr’s disease: familial idiopathic basal ganglia calcification with and without extrapyramidal disorders
Fahr’s disease (FD), also known as familial idiopathic basal ganglia calcification, is a neurodegenerative disease affecting cerebral micro vessels, mainly in the basal ganglia. It mostly presents with movement disorders, dementia and behavioral abnormalities. It is considered hereditary with an autosomal dominant transmission. Fahr’s disease is often underestimated and under diagnosed. We reported the clinical differences found in two patients with Fahr’s Disease. In particular, we described a case of Fahr’s disease with behavioral alteration with extrapyramidal movement disorders, and a rare case of Fahr’s disease with cognitive and behavioral alterations in absence of extrapyramidal movement disorders.
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