Prenatal diagnosis of ring chromosome 6 in a fetus with cerebellar hypoplasia and partial agenesis of corpus callosum: case report and review of the literature

被引:7
|
作者
Andrieux, J [1 ]
Devisme, L
Valat, AS
Robert, Y
Frnka, C
Savary, JB
机构
[1] CHRU, Hop Jean Flandre, Med Genet Lab, F-59037 Lille, France
[2] CHRU Lille, Hop Calmette, Lab Anat & Cytol Pathol, F-59000 Lille, France
[3] CHRU Lille, Hop Jeanne Flandre, Serv Gynecol Obstet, F-59037 Lille, France
[4] CHRU Lille, Hop Jeanne Flandre, Serv Imagerie Med, F-59037 Lille, France
关键词
ring chromosome 6; prenatal diagnosis; corpus callosum agenesis; cerebellar hypoplasia;
D O I
10.1016/j.ejmg.2005.01.028
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Ring chromosome 6 (RC6) is a rare constitutional abnormality, with variable material loss, leading to a variable clinical phenotype: minimal physical anomalies and mild psychomotor retardation to severe physical and mental defects. Among the 22 published cases, only five have been prenatally detected. We describe here a RC6 prenatally diagnosed. Ultrasound follow-up showed growth retardation and cerebellar hypoplasia. Magnetic resonance imaging (MRI) confirmed this, but showed a partial corpus callosum agenesis, leading to amniocentesis and revealing the chromosomal abnormality. Imaging features were correlated with autopsy findings. (c) 2005 Elsevier SAS. All rights reserved.
引用
收藏
页码:199 / 206
页数:8
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