Reflex Seizures Triggered by Diaper Change in Dravet Syndrome

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Reflex Seizures Triggered by Diaper Change in Dravet Syndrome.

Dravet syndrome (DS) is a severe epilepsy syndrome characterized by early onset of multiple types of seizures. We report the first case of reflex seizures triggered by diaper change in a girl at 9 months old and 2 years old with a mutation in the SCN1A gene causing DS. Reflex seizures have been reported in patients with DS provoked by increased body temperature or visual stimulation. The case w...

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Reflex seizures triggered by cutaneous stimuli

PURPOSE Among the different precipitating stimuli for reflex seizures, Touch-Induced Seizures (TIS) and Hot Water Seizures (HWS) are consistently described in different reports. The aim of this study was to analyze the clinical, EEG and image data of patients with TIS and HWS. METHODS We retrospectively analyzed patients who were followed up in our Epilepsy Unit and had seizures triggered by ...

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Occipital seizures induced by Intermittent Photic Stimulation in Dravet syndrome

PURPOSE Dravet syndrome (DS) is a rare disorder with seizure onset in the first year of life, typically beginning with prolonged febrile hemiclonic seizures or generalized tonic-clonic seizures. Photosensitivity is reported in more than 40% of patients. We present two cases of DS in which we had the chance to record occipital seizures induced by Intermittent Photic Stimulation (IPS). METHOD W...

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Dravet syndrome

"Dravet syndrome" (DS) previously named severe myoclonic epilepsy of infancy (SMEI), or epilepsy with polymorphic seizures, is a rare disorder characterized by an early, severe, generalized, epileptic encephalopathy.DS is characterized by febrile and afebrile seizures beginning in the 1st year of life followed by different types of seizures (either focal or generalized), which are typically res...

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Corrigendum to ‘Reflex seizures triggered by cutaneous stimuli’ [Seizure 33 (2015) 72–75]

Corrigendum to ‘Reflex seizures triggered by cutaneous stimuli’ [Seizure 33 (2015) 72–75] J. Sala-Padró *, M. Toledo , S. Sarria , E. Santamarina , M. Gonzalez-Cuevas , M. Sueiras-Gil , J. Salas-Puig a Unitat d’Epilèpsia, Hospital Vall d’Hebrón, Barcelona, Spain b Servei de Neuroradiologia, Hospital Vall d’Hebrón, Barcelona, Spain c Servei de Neurofisiologia, Hospital Vall d’Hebron, Barcelona, ...

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ژورنال

عنوان ژورنال: Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques

سال: 2016

ISSN: 0317-1671,2057-0155

DOI: 10.1017/cjn.2015.394