Searched for "Epilepsy".
146
results
found
on Genetics Home Reference.
Showing results 1 to 20.
- juvenile myoclonic epilepsy condition summary
Found: Juvenile myoclonic epilepsy is a condition characterized by...
- Lafora progressive myoclonus epilepsy condition summary
Found in name or synonym: epilepsy, progressive myoclonic, Lafora
- pyridoxine-dependent epilepsy condition summary
Found in name or synonym: epilepsy, pyridoxine-dependent
- Unverricht-Lundborg disease condition summary
Found in name or synonym: myoclonic epilepsy of Unverricht and Lundborg
- autosomal dominant nocturnal frontal lobe epilepsy condition summary
Found: ...to be an uncommon form of epilepsy; its prevalence is unknown. This...
- autosomal dominant partial epilepsy with auditory features condition summary
Found in name or synonym: Epilepsy, partial, with auditory features
- benign familial neonatal seizures condition summary
Found in name or synonym: benign neonatal epilepsy
- pyridoxal 5'-phosphate-dependent epilepsy condition summary
Found: ...5'-phosphate-dependent epilepsy is a condition that involves seizures...
- myoclonic epilepsy myopathy sensory ataxia condition summary
Found: Myoclonic epilepsy myopathy sensory ataxia, commonly...
- PRICKLE1-related progressive myoclonus epilepsy with ataxia condition summary
Found in name or synonym: progressive myoclonic epilepsy 1B
- dentatorubral-pallidoluysian atrophy condition summary
Found in name or synonym: Myoclonic epilepsy with choreoathetosis
- myoclonic epilepsy with ragged-red fibers condition summary
Found: Myoclonic epilepsy with ragged-red fibers (MERRF)...
Related genes and chromosomes:
- ring chromosome 20 syndrome condition summary
Found in name or synonym: ring chromosome 20 epilepsy syndrome
- Lennox-Gastaut syndrome condition summary
Found: ...syndrome is a form of severe epilepsy that begins in childhood. It is...
- X-linked infantile spasm syndrome condition summary
Found in link title: Epilepsy
- myoclonus epilepsy definition
- ring chromosome 14 syndrome condition summary
Found: ...disability. Recurrent seizures (epilepsy) develop in infancy or early childhood....
- SCN1A gene summary
Official name: sodium channel, voltage-gated, type I, alpha subunit
Found: ...stop by age 5, and generalized epilepsy with febrile seizures plus (GEFS+)....
- EPM2A gene summary
Official name: epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
Found: ...Lafora progressive myoclonus epilepsy. Many of these mutations change...
- NHLRC1 gene summary
Official name: NHL repeat containing 1
Found: ...Lafora progressive myoclonus epilepsy. Many of these mutations change...
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