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Results 1 - 10 of 10 for Focal tonic seizure
  1. SCN2A gene 
    ... gene can cause epilepsy of infancy with migrating focal seizures (EIMFS). This condition is typically characterized by recurrent ... major cause of epilepsy of infancy with migrating focal seizures. Neurology. 2015 Sep 15;85(11):958-66. ...
    https://medlineplus.gov/genetics/gene/scn2a - Genetics
  2. DEPDC5 gene 
    ... epilepsy) that runs in families. Affected individuals experience focal seizures, which are seizures that do not cause a ... an abnormally active mTOR pathway leads to the focal seizures of FFEVF. Research suggests that increased mTOR pathway ...
    https://medlineplus.gov/genetics/gene/depdc5 - Genetics
  3. KCNT1 gene 
    ... in individuals with epilepsy of infancy with migrating focal seizures (EIMFS). This condition is typically characterized by recurrent ...
    https://medlineplus.gov/genetics/gene/kcnt1 - Genetics
  4. SCN1A gene 
    ... provides information about Epilepsy of infancy with migrating focal seizures More About This Health Condition A common change ( ...
    https://medlineplus.gov/genetics/gene/scn1a - Genetics
  5. TSC1 gene 
    ... brain that is responsible for thinking and learning. Focal cortical dysplasia causes severe recurrent seizures (epilepsy) in affected individuals. hamartin KIAA0243 TSC1_HUMAN ...
    https://medlineplus.gov/genetics/gene/tsc1 - Genetics
  6. NPRL2 gene 
    ... gene mutations have been found to cause familial focal epilepsy with variable foci (FFEVF), which is an uncommon form of recurrent seizures (epilepsy) that runs in families. Most of these ...
    https://medlineplus.gov/genetics/gene/nprl2 - Genetics
  7. NPRL3 gene 
    ... gene mutations have been found to cause familial focal epilepsy with variable foci (FFEVF), which is an uncommon form of recurrent seizures (epilepsy) that runs in families. Most of these ...
    https://medlineplus.gov/genetics/gene/nprl3 - Genetics
  8. MTOR gene 
    ... syndrome (described above), the genetic changes that cause focal cortical dysplasia and ... FK506 binding protein 12-rapamycin associated protein 2 ...
    https://medlineplus.gov/genetics/gene/mtor - Genetics
  9. GRIN2A gene 
    ... von Spiczak S. Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes. Nat Genet. 2013 Sep; ... mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction. ...
    https://medlineplus.gov/genetics/gene/grin2a - Genetics
  10. ARX gene 
    ... disability and a group of movement problems called focal dystonia that primarily affects the hands. The most ... callosum), some degree of intellectual disability, and recurrent seizures (epilepsy). Some females with an ARX gene mutation ...
    https://medlineplus.gov/genetics/gene/arx - Genetics