Title of article :
Association of Family History of Epilepsy with Earlier Age Onset of Juvenile Myoclonic Epilepsy
Author/Authors :
Najafi، Mohammad Reza نويسنده Najafi, M.R. , Najafi، Mohammad Amin نويسنده Medical Student Research Center, Isfahan University of Medical Sciences, Isfahan, IR Iran , , SAFAEI، Ali نويسنده Isfahan Neurosciences Research Centre (INRC), Isfahan University of Medical Sciences, Isfahan, Iran ,
Issue Information :
فصلنامه با شماره پیاپی سال 2016
Pages :
6
From page :
10
To page :
15
Abstract :
Abstract Objective Juvenile myoclonic epilepsy (JME) is supposedly the most frequent subtype of idiopathic generalized epilepsies (IGE). The aim of this study was to determine the prevalence of JME and comparison of patients’ demographics as well as timeline of the disease between positive family history epileptic patients (PFHE) and negative family history epileptic patients (NFHE) among sample of Iranian epileptic patients. Materials & Methods From Feb. 2006 to Oct. 2009, 1915 definite epileptic patients (873 females) referred to epilepsy clinics in Isfahan, central Iran, were surveyed and among them, 194 JME patients were diagnosed. JME was diagnosed by its specific clinical and EEG criteria. Patients were divided into two groups as PFHE and NFHE and data were compared between them. Results JME was responsible for 10% (194 patients) of all types of epilepsies. Of JME patients, 53% were female. In terms of family history of epilepsy, 40% were positive. No significant differences was found between PFHE and NFHE groups as for gender (P > 0.05). Age of epilepsy onset was significantly earlier in PFHE patients (15 vs. 22 yr, P < 0.001). Occurrence of JME before 18 yr old among PFHE patients was significantly higher (OR=2.356, P=0.007). Conclusion A family history of epilepsy might be associated with an earlier age of onset in patients with JME.
Journal title :
Iranian Journal of Child Neurology (IJCN)
Serial Year :
2016
Journal title :
Iranian Journal of Child Neurology (IJCN)
Record number :
2399169
Link To Document :
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