Extensive brain calcification in two children with bilateral Coats' disease

被引：20

作者：

Goutières, F

Dollfus, H

Becquet, F

Dufier, JL

机构：

[1] Hop Necker Enfants Malad, Pediat Neurol Unit, F-75743 Paris 15, France

[2] Hop Necker Enfants Malad, Dept Ophthalmol, F-75743 Paris, France

来源：

NEUROPEDIATRICS | 1999年 / 30卷 / 01期

关键词：

Coats' retinopathy; basal ganglia calcifications; cerebellar ataxia;

D O I：

10.1055/s-2007-973451

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

We report two children with bilateral Coats' disease associated with cerebral calcifications in the basal ganglia and deep white matter, asymptomatic at the time of their discovery. Cerebellar ataxia developed secondarily in one of them. Both children were born small for date and had febrile convulsive seizures. Three similar patients have been previously reported, two of them in the same sibship: the third reported patient died of aplastic anemia. Bilateral Coots' disease in children should prompt systematic CT scan in search of cerebral calcifications. If present, neurological and genetic prognosis should be cautious.

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页码：19 / 21

页数：3

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