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PedAM

Pediatric Disease Annotations & Medicines




Disease epilepsy
Symptom C0270846|atonic seizures
Sentences 9
PubMedID- 25865495 Mutations in the gaba transporter slc6a1 cause epilepsy with myoclonic-atonic seizures.
PubMedID- 22424762 We review the effectiveness of the kd in dravet syndrome, epilepsy with myoclonic-atonic seizures, mitochondrial disease, tuberous sclerosis, late infantile and juvenile neuronal ceroid lipofuscinosis, and febrile infection-related epilepsy syndrome.
PubMedID- 23936641 In this paper, we review the use of the ketogenic diet in epileptic encephalopathies such as ohtahara syndrome, west syndrome, dravet syndrome, epilepsy with myoclonic atonic seizures, and lennox-gastaut syndrome.
PubMedID- 23583052 epilepsy with myoclonic-atonic seizures is characterized by myoclonic-atonic, absence, tonic-clonic, and eventually tonic seizures, appearing in previously normal children at ages 18-60 months.
PubMedID- 26133327 Doose syndrome, or epilepsy with myoclonic-atonic seizures, is a rare electroclinical syndrome.
PubMedID- 25884503 It was recently renamed as epilepsy with myoclonic-atonic seizures and classified as one of the childhood onset electroclinical syndromes 6.
PubMedID- 25532859 One, carrying a novel de novo deletion had epilepsy with myoclonic-atonic seizures (mae), mild slowing of head growth, choreiform movements and developmental delay.
PubMedID- 23531455 We present findings observed in a patient with atonic seizures due to focal epilepsy, who underwent intracranial video-eeg monitoring and epilepsy surgery, and discuss possible underlying mechanisms.
PubMedID- 26262932 Chd2 mutations are a rare cause of generalized epilepsy with myoclonic-atonic seizures.

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