Corrigendum to “Do pure absence seizures occur in myoclonic epilepsy of infancy? A case series” [Seizure: Eur. J. Epilepsy 24 (2015) 8–11]
نویسندگان
چکیده
Vincenzo Belcastro *, Lucio Giordano , Dario Pruna , Cinzia Peruzzi , Francesco Madeddu , Patrizia Accorsi , Giuseppe Gobbi , Alberto Verrotti , Pasquale Striano g Neurology Unit, Department of Medicine, S. Anna Hospital, Como, Italy b Pediatric Neuropsychiatric Division, Spedali Civili, Brescia, Italy c Epilepsy Unit, Child Neuropsychiatry Department, University Hospital, Cagliari, Italy Department of Paediatrics, University of Novara, Italy e Child Neurology Unit, Bellaria Hospital, IRCCS lstituto delle Scienze Neurologiche, Bologna, Italy Department of Pediatrics, University of Perugia, Italy g Pediatric Neurology and Muscular Diseases Unit, Department of Neurosciences, Rehabilitation, Ophtalmology, Genetics, Maternal and Child Health, University of Genoa, ‘‘G. Gaslini’’ Institute, Genova, Italy
منابع مشابه
Do pure absence seizures occur in myoclonic epilepsy of infancy? A case series
PURPOSE To assess if absence seizures (ASs) occur in patients with myoclonic epilepsy of infancy (MEI). METHODS A retrospective chart review was conducted in 37 patients with MEI followed at seven different paediatric epilepsy centres in Italy, between 2002 and 2014. To assess the possible occurrence of pure ASs or absences associated with myoclonias, ASs were defined according to the followi...
متن کاملSevere myoclonic epilepsy in infancy: evolution of seizures
Changes in seizure type of severe myoclonic epilepsy (SME) in infancy were reviewed retrospectively in 14 patients (11 males and 3 females) who were followed-up to the age of 7 years or more. The observation period ranged from 5 to 16 years with a mean of 10 years. During the follow-up, three or four types of seizures were seen per patient, but the pattern of appearance and disappearance of eac...
متن کاملA patient with myoclonic epilepsy in infancy followed by myoclonic astatic epilepsy
Myoclonic epilepsy in infancy (MEI) is a primary generalized epilepsy. According to the literature, the outcome of MEI is usually benign. Here we report a patient who developed myoclonic astatic epilepsy at age four, having been seizure free without antiepileptic drug treatment for 2 years after his recovery from MEI. At age four, a video-EEG-recording showed frequent head nodding (atonic seizu...
متن کاملEpilepsy syndromes in infancy.
An increasing number of infantile epilepsy syndromes have been recognized. However, a significant number of infants (children aged 1-24 months) do not fit in any of the currently used subcategories. This article reviews the clinical presentation, electroencephalographic findings, evolution, and management of the following entities: early infantile epileptic encephalopathy, early myoclonic epile...
متن کاملO 23: Anti-Inflammatory Treatment in Children with Refractory Seizure
Epilepsy is a neurological disease of the central nervous system. It is estimated that about 50-70 million people worldwide suffer from this chronic disorder and 20 to 30% are resistant to conventional anti-epileptic drugs. In the epilepsy therapeutic arena, there is real need for developing novel antiepileptogenesis treatments that offer a way to prevent the onset or the progression of the dis...
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ورودعنوان ژورنال:
- Seizure
دوره 30 شماره
صفحات -
تاریخ انتشار 2015