Results 1 -
10
of
190
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Rare genetic epilepsy
- ... myoclonus epilepsy type 1 ULD Unverricht-Lundborg syndrome Genetic Testing Registry: Unverricht-Lundborg syndrome Progressive myoclonic epilepsy type 1 National Organization for Rare Disorders (NORD) MYOCLONIC EPILEPSY OF UNVERRICHT AND LUNDBORG ...
- ... myoclonic epilepsy 1B Progressive myoclonus epilepsy with ataxia Genetic Testing Registry: Epilepsy, progressive myoclonic, 1B National Organization for Rare Disorders (NORD) EPILEPSY, PROGRESSIVE MYOCLONIC, 1B; EPM1B PubMed ...
- ... factors contribute to development of the condition. Most genetic changes associated with childhood absence epilepsy are rare, having been found in only a small number ...
- ... nephropathy syndrome Progressive myoclonus epilepsy with renal failure Genetic Testing Registry: Action myoclonus-renal failure syndrome National Organization for Rare Disorders (NORD) EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE; ...
- ... the condition. MEMSA SCAE Spinocerebellar ataxia with epilepsy Genetic Testing Registry: Spinocerebellar ataxia with epilepsy National Organization for Rare Disorders (NORD) ClinicalTrials.gov SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, ...
- ... epilepsy type 2 Progressive myoclonus epilepsy, Lafora type Genetic Testing Registry: Lafora disease Lafora disease National Organization for Rare Disorders (NORD) ClinicalTrials.gov MYOCLONIC EPILEPSY OF LAFORA 1; MELF1 PubMed Andrade DM, Turnbull ...
- ... ragged-red fibers Myoencephalopathy ragged-red fiber disease Genetic Testing Registry: MERRF syndrome MERRF National Organization for Rare Disorders (NORD) ClinicalTrials.gov MYOCLONIC EPILEPSY ASSOCIATED WITH RAGGED-RED FIBERS; MERRF PubMed Blakely ...
- ... Testing Registry: Epilepsy, idiopathic generalized, susceptibility to, 9 Genetic Testing Registry: Juvenile myoclonic epilepsy Juvenile myoclonic epilepsy National Organization for Rare Disorders (NORD) ClinicalTrials.gov EPILEPSY, MYOCLONIC JUVENILE; EJM ...
- ... seizures Pyridoxine-dependent seizures Vitamin B6-dependent seizures Genetic Testing Registry: Pyridoxine-dependent epilepsy Pyridoxine-dependent epilepsy National Organization for Rare Disorders (NORD) ClinicalTrials.gov EPILEPSY, EARLY-ONSET, 4, ...
- Tuberous Sclerosis Complex (National Institute of Neurological Disorders and Stroke)Tuberous Sclerosis/Start Here ... Tuberous Sclerosis ... National Institute of Neurological Disorders and Stroke ... Tuberous sclerosis complex (TSC), also known as tuberous ...