International Journal of Epilepsy

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Psychosocial care needs of the parents having children with epilepsy
International Journal of Epilepsy - Tập 1 - Trang 21-26 - 2014
Ramu Rajalakshmi, Krishnasamy Lalitha
Plasma tetranectin as a potential clinical biomarker for epilepsy and correlation with clinical and social characteristics
International Journal of Epilepsy - Tập 4 - Trang 2-5 - 2017
Ekta Singh Dahiya, Man Mohan Mehndiratta, Krishna Kolappa Pillai
Abstract Background Tetranectin concentration has been identified as a biomarker of several types of metastatic and malignant cancers. The role of tetranectin has also be seen in some neurological disorders. We aimed to estimate the plasma tetranectin concentration in different groups of people with epilepsy (PWE) followed-up for a year. As a secondary objective, the clinical and social characteri... hiện toàn bộ
Time to treatment predicts seizure outcome in a high-treatment gap epilepsy population
International Journal of Epilepsy - Tập 2 - Trang 72-77 - 2015
Michael B. Fawale, Mayowa O. Owolabi, Adekunle F. Mustapha, Morenikeji A. Komolafe, Ogunniyi Adesola
Abstract Objectives To investigate the relationship between time to antiepileptic drug (AED) treatment (TTT) and seizure outcome in a high treatment gap sub-Sahara African setting. Methods Clinical and demographic characteristics of 72 adults with epilepsy aged 18–75 years were obtained. We estimated TTT as the difference between the duration of epilepsy and the duration of treatment. Indices of c... hiện toàn bộ
A child with global neuroregression with refractory epilepsy
International Journal of Epilepsy - Tập 1 - Trang 92-93 - 2014
Rachana Dubey, Biswaroop Chakrabarty, Sheffali Gulati, Atin Kumar
AbstractHypomyelinating disorders have wide spectrum of clinical and radiological manifestations. A 17-month-old girl presented with baseline global developmental delay with insidious onset global neuroregression with refractory seizures from 1 year of age. Her birth and family history were noncontributory. Salient features on examination were central hypotonia and retinal cherry red spot. MRI Bra... hiện toàn bộ
Clinical, MRI and electrographic characteristics of three children with Hemiconvulsion-Hemiplegia/Hemiconvulsion-Hemiplegia-Epilepsy (HH/HHE) syndrome–A rare childhood epileptic encephalopathy
International Journal of Epilepsy - Tập 4 - Trang 79-86 - 2017
Yeeshu Singh Sudan, K.P. Vinayan, Arun Grace Roy
AbstractHemi convulsion-Hemiplegia-Epilepsy (HH/HHE) syndrome is a very rare catastrophic epileptic syndrome in childhood which follows a prolonged focal motor status epilepticus in infancy and early childhood. Here we are describing the clinical, MRI and electrographic characteristics along with long term outcome of three children with HH/HHE syndrome. A review of the current literature on HH/HHE... hiện toàn bộ
Batwing appearance – A neuroradiologic clue to glutaric aciduria-type 1
International Journal of Epilepsy - Tập 2 - Trang 44-48 - 2015
Anusha Doraiswamy, Bhanu Kesavamurthy, Lakshminarasimhan Ranganathan
AbstractGlutaric aciduria type 1 (GA-1) is a rare inherited neurometabolic disorder due to enzymatic block in the common degradation pathway for lysine and tryptophan. We report a 16 month girl child who presented with an initial acute encephalopathic crisis followed by static encephalopathy with characteristic neuroimaging findings. Diagnosis was confirmed by demonstrating elevated urinary glutar... hiện toàn bộ
Evaluation of DNA damage and mutation screening of exon 26 of SCN1A gene in patients with epilepsy
International Journal of Epilepsy - Tập 4 - Trang 125-131 - 2017
Nishu Sekar, Shalaka Ramgir, Yogamaya D Prabhu, Kaviyarasi Renu, Abilash V.G
Abstract Background Epilepsy is one of the most prevalent neurological disorders. Around 50 million people worldwide suffer from Epilepsy, 85% of them are from the developing countries. It is a most significant as well as common brain disorder worldwide. Sodium channel alpha 1 subunit gene (SCN1A) is most commonly mutated the gene in different forms of epilepsy. Objective To screen the genomic dam... hiện toàn bộ
Neonatal seizures and epilepsies
International Journal of Epilepsy - Tập 1 - Trang 75-83 - 2014
Kollencheri Puthenveettil Vinayan, Solomon L. Moshé
AbstractNeonatal seizure is the most frequent clinical manifestation of central nervous system dysfunction in the newborn. It is defined as a paroxysmal alteration in neurologic function that include motor, behavior and/or autonomic functions occurring in the first 28 days after birth of a term neonate or before 44 weeks of gestational age in a preterm infant. Seizures in the presence of encephalo... hiện toàn bộ
A case of paroxysmal nocturnal dystonia responsive to cyproheptadine: Is it almost always epileptic?
International Journal of Epilepsy - Tập 2 - Trang 49-50 - 2015
Mohammad Sayadnasiri
AbstractNocturnal Paroxysmal Dystonia (NPD) is characterized by abnormal dyskinetic movements occur mostly during non-REM sleep. From introducing NPD in early 1980s, most authors have been in favour of an epileptic origin for these sleep-related episodes. Clinical characteristics of NPD including abrupt hypermotor behaviours, automatisms and vocalizations, abnormal EEG findings in some patients an... hiện toàn bộ
Cognitive deficits in the first 24 hours after the onset of first unprovoked generalized Tonic and clonic seizure
International Journal of Epilepsy - Tập 4 - Trang 141-143 - 2017
Zeinab Charmchi, Mohammad Sayadnasiri
AbstractBackground Many people with epilepsy suffer from cognitive deficits as a consequence of their seizure episodes. Relatively few researches have been undertaken to assess the short term impacts of seizure on cognitive function. This study aimed to evaluate changes in cognitive performance in adults with a new onset generalized seizure in the first 24 h after the onset of their attack.Methods... hiện toàn bộ
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