ArticleIranian journal of child neurology2016
Association of Family History of Epilepsy with Earlier Age Onset of Juvenile Myoclonic Epilepsy.
Article in Iranian journal of child neurology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
What it found
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Who cites it
5 citing papers in PubMed.
- Demographics, Clinical Characteristics, and Management Strategies of Epilepsy in Saudi Arabia: A Systematic Review.Cureus · 2024Review
- Evaluating the Inheritance Risk: Epilepsy Prevalence among Offspring of Adults with Epilepsy in a Tertiary Referral Epilepsy Center.Journal of clinical medicine · 2024Article
- Risk factors for secondary epilepsy in children with complex febrile seizures and their effect on growth and development-a retrospective cohort study.Translational pediatrics · 2023Article
- Causes and Risk Factors of Drug-Resistant Epilepsy in Children.Iranian journal of child neurology · 2023Article
- Vitamin B12 and Folate Status in Patients with Epilepsy Under Levetiracetam Monotherapy.International journal of preventive medicine · 2019Article
Corrections and comments
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Authors and funding
3 authors.
Funding
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Abstract
objectiveJuvenile 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 &
methodsFrom 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.
resultsJME 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).
conclusionA family history of epilepsy might be associated with an earlier age of onset in patients with JME.
Indexed as
Identifiers
27247579PMC4885150What OpenQuestion holds
Registered trials
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