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家族性特发性纹状体苍白球齿状核钙化

Familial idiopathic striopallidodentate calcifications.

作者信息

Ellie E, Julien J, Ferrer X

机构信息

Département de Neurologie, Hopital du Haut-Lévêque, Pessac, France.

出版信息

Neurology. 1989 Mar;39(3):381-5. doi: 10.1212/wnl.39.3.381.

Abstract

We report a father and son with striopallidodentate calcifications. Metabolic studies excluded calcium/phosphorus metabolism disturbances and no specific etiology was found. The structure of the calcified areas differed, on magnetic resonance imaging, depending on location and, probably, age. There are nine families with similar clinical and radiologic backgrounds and no evident etiology in the literature. Transmission is most often autosomal dominant, and in contrast with physiologic senescent basal ganglia calcification, the prognosis appears to be poor.

摘要

我们报告了一对患有纹状体苍白球齿状核钙化的父子。代谢研究排除了钙/磷代谢紊乱,未发现特定病因。在磁共振成像上,钙化区域的结构因位置不同而有所差异,可能还与年龄有关。文献中有九个家族具有相似的临床和放射学背景且病因不明。遗传方式多为常染色体显性遗传,与生理性衰老的基底节钙化不同,其预后似乎较差。

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