Costello syndrome and neurological abnormalities

被引:41
作者
Delrue, MA
Chateil, JF
Arveiler, B
Lacombe, D
机构
[1] CHU Pellegrin Enfants, Serv Genet Med, Dept Med Genet, F-33076 Bordeaux, France
[2] CHU Pellegrin Enfants, Dept Pediat Radiol, F-33076 Bordeaux, France
来源
AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 2003年 / 123A卷 / 03期
关键词
Costello syndrome; neurological abnormalities;
D O I
10.1002/ajmg.a.20330
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Costello syndrome is a rare but increasingly recognized syndrome of unknown etiology. Neurological abnormalities are not rare in this syndrome and consist of structural and electrophysiological disorders. Ventricular dilatation is observed in more than 40% of cases. Other reported cerebral anomalies are brain atrophy, Chiari malformation and syringomyelia. Although there is insufficient data to propose strict guidelines, it seams reasonnable to have a low threshold for neuroimaging, in general, and particularly when neurologic signs or symptoms are present. Screening including cerebral MRI and EEG should be proposed after a diagnosis of Costello syndrome. The frequency of testing in such children should be guided by neurological follow-up. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:301 / 305
页数:5
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