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PedAM

Pediatric Disease Annotations & Medicines




Disease dystonia
Phenotype C0014544|epilepsy
Sentences 5
PubMedID- 26245188 Psychogenic non-epileptic seizures, sleep disorders, syncope, dystonia), patients with a doubtful epilepsy diagnosis, patients who had only a single seizure, and patients with a severe mental retardation.
PubMedID- 22613698 Steroid-responsive focal epilepsy with focal dystonia accompanied by glutamate receptor delta2 antibody.
PubMedID- 20213496 The tottering phenotype, an autosomal recessive mouse disease, is associated with mild ataxia, spontaneous behavioral arrest associated with synchronous, bilateral cortical polyspike discharges (resembling human absence epilepsy), and attacks of paroxysmal dystonia [10, 61].
PubMedID- 26088892 Myoclonic occipital photosensitive epilepsy with dystonia (moped): a familial epilepsy syndrome.
PubMedID- 21087195 Early-onset progressive myoclonic epilepsy with dystonia mapping to 16pter-p13.3.

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