eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | juvenile myoclonic epilepsy |
| Symptom | C0036572|seizures |
| Sentences | 7 |
| PubMedID- 25767482 | Based on the age of onset and seizure type, ige can be divided into four syndromes according to the still valid classification of the international league against epilepsy: childhood absence epilepsy, occurring after the neonatal period; juvenile absence epilepsy; juvenile myoclonic epilepsy; and ige with tonic–clonic seizures alone4. |
| PubMedID- 25950944 | Disease phenotype: asd: autism spectrum disorder, adhd: attention deficit hyperactivity disorder, an: anorexia nervosa, aut: autism, bpd: bipolar disorder, ee: epileptic encephalopathy, epi: epilepsy, id: intellectual disability, mcp: microcephaly, scz: schizophrenia; gge syndromes: cae: childhood absence epilepsy, jae: juvenile absence epilepsy, jme: juvenile myoclonic epilepsy, egma: epilepsy with generalised tonic-clonic seizures alone predominantly on awakening, egtcs: epilepsy with generalised tonic-clonic seizures alone, gsw: generalised spike and wave discharges on the electroencephalogram, number/: age-at-onset of afebrile generalised seizures. |
| PubMedID- 25250802 | Sleep deprivation is an important provoker of seizures in juvenile myoclonic epilepsy. |
| PubMedID- 23986742 | The oral form has food and drug administration (fda) indications for adjunctive therapy in the treatment of partial onset epilepsy ages 1 month or more, myoclonic seizures associated with juvenile myoclonic epilepsy starting with the age of 12 and primary generalized tonic-clonic seizures in people 6 years and older. |
| PubMedID- 21151621 | Myoclonic seizures occur usually in patients with juvenile myoclonic epilepsy. |
| PubMedID- 20087210 | Latencies were significantly shorter in juvenile absence epilepsy than in juvenile myoclonic epilepsy, epilepsy with generalized tonic-clonic seizures only, and ige not further classified (p = 0.001). |
| PubMedID- 24883310 | In 2011, liu investigated the wm differences between normal controls and two subsets of ige, juvenile myoclonic epilepsy and ige with generalized tonic-clonic seizures only. |
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