Rhombencephalosynapsis diagnosed in childhood: Clinical and MRI findings

被引：20
|
作者：
Danon, O [1 ]
Elmaleh, M [1 ]
Boukobza, B [1 ]
Fohlen, M [1 ]
Hadjnacer, K [1 ]
Hassan, M [1 ]
机构：
[1] Laennec Hosp, Dept Radiol, F-60100 Creil, France
来源：
MAGNETIC RESONANCE IMAGING | 2000年 / 18卷 / 01期
关键词：
rhombencephalosynapsis; cerebellar abnormalities; cranial fossa; posterior;
D O I：
10.1016/S0730-725X(99)00113-7
中图分类号：
R8 [特种医学]; R445 [影像诊断学];
学科分类号：
1002 ; 100207 ; 1009 ;
摘要：
Rhombencephalosynapsis is an unfrequent malformation of the posterior fossa essentially characterized by vermian agenesis or hypogenesis, fusion of the cerebellar hemispheres and fusion of the dentate nuclei. Supratentorial abnormalities are usually associated. No specific clinical syndrome can be described in relation with this disorder. We report a case diagnosed by MRI in a Living patient. (C) 2000 Elsevier Science Inc. All rights reserved.
引用
收藏
页码：99 / 101
页数：3
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