Lobar holoprosencephaly: prenatal MR diagnosis with postnatal MR correlation

被引:5
|
作者
Wong, AMC
Bilaniuk, LT
Ng, KK
Chang, YL
Chao, AS [1 ]
Wai, YY
机构
[1] Chang Gung Mem Hosp, Dept Diagnost Radiol, Taoyuan 333, Taiwan
[2] Childrens Hosp Philadelphia, Dept Diagnost Radiol, Philadelphia, PA 19104 USA
关键词
lobar holoprosencephaly; prenatal diagnosis; MRI;
D O I
10.1002/pd.1108
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Holoprosencephaly is a congenital anomaly characterized by lack of cleavage of the prosencephalon. Although, relatively rare, it is the most common anomaly that involves both the brain and the face. Prenatal diagnosis of this anomaly using ultrasonography, particularly of the less severe forms, is difficult. Magnetic resonance imaging has recently become an important complement to US in prenatal diagnosis of CNS anomalies. We herein report a patient in whom, at 23 weeks of gestation, US suggested agenesis of the corpus callosum and in whom, at 24 weeks of gestation, MRI correctly diagnosed lobar holoprosencephaly, which was confirmed by a postnatal MRI at 3 weeks of age. Copyright © 2005 John Wiley & Sons, Ltd.
引用
收藏
页码:296 / 299
页数:4
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