Focal polymicrogyria in mother and son

被引:19
作者
Caraballo, RH [1 ]
Cersósimo, RO [1 ]
Mazza, E [1 ]
Fejerman, N [1 ]
机构
[1] Hosp Nacl Pediat Prof Dr Juan P Garrahan, Dept Neurol, RA-1245 Buenos Aires, DF, Argentina
关键词
familial focal polymicrogyria; cerebral migrational and organizational disorder; epilepsy; congenital hemiparesis; magnetic resonance imaging;
D O I
10.1016/S0387-7604(00)00125-X
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
This 9-year-old boy was admitted at the age of 2 with a diagnosis of congenital hemiparesis while the rest of physical and neurological examination was normal. His score in the Wechsler intelligence scale was 80. Right fronto-parietal cortical dysplasia with hemisphere atrophy was evident by computerized tomography scanning and magnetic resonance imaging. The latter, also disclosed abnormal thick cortex which was interpreted as polymicrogyria or pachygyria. Karyotype was normal. We had a hemifacial motor seizure at the age of 7. At the age of 8 frequent atonic or inhibitory seizures were presented. Asymmetric bilateral spike discharges with high voltage in the right hemisphere during the EEG recording were found. His mother, a 35-year-old woman (Full scale, Adult intelligence scale: 85) also had congenital hemiparesis. She never had seizures and her EEG was normal. Magnetic resonance imaging disclosed right fronto-parietal cortical dysplasia with ipsilateral hemisphere atrophy. Karyotype was normal. Our casts should he interpreted us a familial presentation of the anomaly, probably with autosomal-dominant transmission. (C) 2000 Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:336 / 339
页数:4
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