FAMILIAL DANDY-WALKER MALFORMATION ASSOCIATED WITH MACROCEPHALY, FACIAL ANOMALIES, DEVELOPMENTAL DELAY, AND BRAIN-STEM DYSGENESIS - PRENATAL-DIAGNOSIS AND POSTNATAL OUTCOME IN BROTHERS - A NEW SYNDROME

被引:29
作者
CHITAYAT, D
MOORE, L
DELBIGIO, MR
MACGREGOR, D
BENZEEV, B
HODGKINSON, K
DECK, J
STOTHERS, T
RITCHIE, S
TOI, A
机构
[1] UNIV TORONTO,HOSP SICK CHILDREN,DEPT PEDIAT,DIV NEUROL,TORONTO M5G 1X8,ON,CANADA
[2] TORONTO HOSP,DEPT PATHOL,TORONTO M5T 2S8,ON,CANADA
[3] TORONTO HOSP,DEPT RADIOL,TORONTO M5T 2S8,ON,CANADA
[4] TORONTO HOSP,PRENATAL DIAG PROGRAM,TORONTO M5T 2S8,ON,CANADA
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1994年 / 52卷 / 04期
关键词
INHERITED; X-LINKED RECESSIVE; AUTOSOMAL RECESSIVE; ULTRASOUND;
D O I
10.1002/ajmg.1320520404
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Brothers are reported with an apparently new constellation of manifestations including Dandy-Walker complex (DWC), migrational brain disorder, macrocephaly, and facial anomalies. The first brother presented at birth, the second was detected prenatally with DWC and the pregnancy terminated. Fetal brain histopathology showed DWC associated with brainstem dysgenesis. Inheritance is likely autosomal or X-linked recessive. An extensive review of the differential diagnosis of DWC is provided. (C) 1994 Wiley-Liss, Inc.
引用
收藏
页码:406 / 415
页数:10
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