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Results 1 - 4 of 4 for Myoclonic epilepsy in infancy
Did you mean mayoclinic epilepsy in infancy?
  1. SCN1A gene 
    ... such as Dravet syndrome (also known as severe myoclonic epilepsy of infancy or SMEI), that cause more serious seizures that ... Clinical spectrum of mutations in SCN1A gene: severe myoclonic epilepsy in infancy and related epilepsies. Epilepsy Res. 2006 Aug;70 ...
    https://medlineplus.gov/genetics/gene/scn1a - Genetics
  2. GABRA1 gene 
    ... identified in at least one family with juvenile myoclonic epilepsy. This condition typically begins in childhood or adolescence ... GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy. Nat Genet. 2002 Jun;31(2):184-9. ...
    https://medlineplus.gov/genetics/gene/gabra1 - Genetics
  3. TBC1D24 gene 
    ... people with other seizure disorders, including familial infantile myoclonic epilepsy (FIME) and progressive myoclonus epilepsy (PME). These mutations ...
    https://medlineplus.gov/genetics/gene/tbc1d24 - Genetics
  4. MT-TK gene 
    ... TK gene have been identified in people with myoclonic epilepsy with ragged-red fibers (MERRF). This condition is ...
    https://medlineplus.gov/genetics/gene/mt-tk - Genetics