SCIENTIFIC BACKGROUND

CHRNA2, KCNQ2, KCNQ3, PRRT2, SCN2A, SCN8A

  • Benign familial infantile seizures (BFIS) CHRNA2)
  • BFIS2 (PRRT2)
  • BFIS3 (SCN2A)
  • BFIS5 (SCN8A)
  • Benign familial neonatal seizures 1 (BFNS1) (KCNQ2)
  • BFNS2 (KCNQ3)

 

Disorders are inherited in an autosomal dominant pattern. Genes in bold are core genes.

 

For detailed information on epilepsies and diagnostics, please visit our overview page EPILEPSY.

GENES
CHRNA2, KCNQ2, KCNQ3, PRRT2, SCN2A, SCN8A
ASSOCIATED TESTS
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