Document Detail


Epilepsy in Rett syndrome: Clinical and genetic features.
MedLine Citation:
PMID:  20728410     Owner:  NLM     Status:  In-Data-Review    
Abstract/OtherAbstract:
Epilepsy often occurs in Rett syndrome and is considered a major problem. The aim of this study was to define the clinical features of epilepsy and the correlation between seizures and both genotype and clinical phenotype in the Rett population. One hundred sixty-five patients with Rett syndrome referred to four Italian centers were recruited. All patients underwent video/EEG monitoring and molecular analysis of the MECP2 gene or, in negative cases, of the CDKL5 and FOXG1 genes. The frequency of epilepsy was 79%. Drug-resistant epilepsy occurred in 30% of all our patients with Rett syndrome and in 38% of those with epilepsy. Our findings demonstrate that epilepsy differs among the various phenotypes and genotypes with respect to age at onset, drug responsiveness, and seizure semiology. The Hanefeld and preserved speech variants represent the extremes of the range of severity of epilepsy: the preserved speech variant is characterized by the mildest epileptic phenotype as epilepsy is much less frequent, starts later, and is less drug resistant than what is observed in the other phenotypes. Another important finding is that seizure onset before 1year of age and daily frequency are risk factors for drug resistance. Thus, this study should help clinicians provide better clinical counseling to the families of patients with Rett syndrome.
Authors:
Maria Pintaudi; Maria Grazia Calevo; Aglaia Vignoli; Elena Parodi; Francesca Aiello; Maria Giuseppina Baglietto; Yussef Hayek; Sabrina Buoni; Alessandra Renieri; Silvia Russo; Francesca Cogliati; Lucio Giordano; Mariapaola Canevini; Edvige Veneselli
Publication Detail:
Type:  Journal Article     Date:  2010-08-21
Journal Detail:
Title:  Epilepsy & behavior : E&B     Volume:  19     ISSN:  1525-5069     ISO Abbreviation:  Epilepsy Behav     Publication Date:  2010 Nov 
Date Detail:
Created Date:  2010-12-14     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  100892858     Medline TA:  Epilepsy Behav     Country:  United States    
Other Details:
Languages:  eng     Pagination:  296-300     Citation Subset:  IM    
Copyright Information:
Copyright © 2010 Elsevier Inc. All rights reserved.
Affiliation:
Department of Child Neuropsychiatry, Epilepsy Centre, G. Gaslini Institute, University of Genoa, Genoa, Italy.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  The emerging genetics of type 2 diabetes.
Next Document:  Study of DSM-IV Axis I psychiatric disorders in patients with refractory complex partial seizures us...