BRAIN MAGNETIC-RESONANCE-IMAGING FINDINGS IN THE OPITZ G/BBB SYNDROME - EXTENSION OF THE SPECTRUM OF MIDLINE BRAIN ANOMALIES

被引:15
作者
MACDONALD, MR
SCHAEFER, GB
OLNEY, AH
TAMAYO, M
FRIAS, JL
机构
[1] UNIV NEBRASKA,MED CTR,HATTIE B MUNROE CTR HUMAN GENET,MEYER REHABIL INST,DEPT PEDIAT,OMAHA,NE 68198
[2] UNIV JAVERIANA,FAC MED,BOGOTA,COLOMBIA
[3] UNIV S FLORIDA,DEPT PEDIAT,TAMPA,FL 33620
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1993年 / 46卷 / 06期
关键词
MIDLINE FIELD DEFECT; COMPUTERIZED IMAGE ANALYSIS; CEREBRAL DYSGENESIS;
D O I
10.1002/ajmg.1320460622
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We report the brain magnetic resonance imaging findings in 4 patients with the Opitz BBB/G syndrome. The scans were assessed by subjective interpretation and computerized image analysis. Findings noted in 3 of the 4 patients include hypoplasia or agenesis of the corpus callosum (3 patients), cerebellar vermal hypoplasia (2 patients), cortical atrophy and ventriculomegaly (3 patients), macro cisterna magna (3 patients), and a wide cavum septum pellucidum (1 patient). One patient had a normal scan. The demonstration of a wide cavum septum pellucidum extends the spectrum of midline brain anomalies (ventral induction defects) reported in this condition. This study along with other recent reports suggests that midline brain anomalies may be frequent findings in Opitz syndrome. (C) 1993 Wiley-Liss, Inc.
引用
收藏
页码:706 / 711
页数:6
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