Epilepsy and chromosomal abnormalities

被引:21
|
作者
Sorge, Giovanni [1 ]
Sorge, Anna [1 ]
机构
[1] Univ Catania, Dept Pediat, Azienda Osped Univ Policlin Vittorio Emanuele, I-95123 Catania, Italy
关键词
WOLF-HIRSCHHORN-SYNDROME; FRAGILE-X-SYNDROME; PALLISTER-KILLIAN-SYNDROME; 1P36 DELETION SYNDROME; DOWN-SYNDROME; RING CHROMOSOME-20; TERMINAL DELETION; ANGELMAN-SYNDROME; MOLECULAR CHARACTERIZATION; INTRACTABLE EPILEPSY;
D O I
10.1186/1824-7288-36-36
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background: Many chromosomal abnormalities are associated with Central Nervous System (CNS) malformations and other neurological alterations, among which seizures and epilepsy. Some of these show a peculiar epileptic and EEG pattern. We describe some epileptic syndromes frequently reported in chromosomal disorders. Methods: Detailed clinical assessment, electrophysiological studies, survey of the literature. Results: In some of these congenital syndromes the clinical presentation and EEG anomalies seems to be quite typical, in others the manifestations appear aspecific and no strictly linked with the chromosomal imbalance. The onset of seizures is often during the neonatal period of the infancy. Conclusions: A better characterization of the electro clinical patterns associated with specific chromosomal aberrations could give us a valuable key in the identification of epilepsy susceptibility of some chromosomal loci, using the new advances in molecular cytogenetics techniques - such as fluorescent in situ hybridization (FISH), subtelomeric analysis and CGH (comparative genomic hybridization) microarray. However further studies are needed to understand the mechanism of epilepsy associated with chromosomal abnormalities.
引用
收藏
页数:8
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