Familial myoclonic epilepsy syndrome: types
Evidence-based neurology checklist on familial myoclonic epilepsy syndrome: types: Familial myoclonic epilepsy syndromes Benign adult familial myoclonic epilepsy (BAFME) Familial adult myoclonic epilepsy (FAME) Familial cortical myoclonus (FCM) Autosomal dominant cortical myoclonus and epilepsy…
Familial myoclonic epilepsy syndromes
- Benign adult familial myoclonic epilepsy (BAFME)
- Familial adult myoclonic epilepsy (FAME)
- Familial cortical myoclonus (FCM)
- Autosomal dominant cortical myoclonus and epilepsy (ADCME)
- Familial cortical myoclonic tremor and epilepsy (FCMTE)
- Autosomal recessive cortical myoclonic tremor and epilepsy
References
- Stogmann E, Reinthaler E, Eltawil S, et al. Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2. Brain 2013; 136:1155-1160.
- Yeetong P, Ausavarat S, Bhidayasiri R, et al. A newly identified locus for benign adult familial myoclonic epilepsy on chromosome 3q26.32-3q28. Eur J Hum Genet 2013; 21:225-228.
- de Falco FA, Striano P, de Falco A, et al. Benign adult familial myoclonic epilepsy: genetic heterogeneity and allelism with ADCME. Neurology 2003; 60:1381-1385.
- Plaster NM, Uyama E, Uchino M, Ikeda T, Flanigan KM, Kondo I, Ptácek LJ. Genetic localization of the familial adult myoclonic epilepsy (FAME) gene to chromosome 8q24. Neurology 1999; 53:1180-1183.
- Labauge P, Amer LO, Simonetta-Moreau M, et al. Absence of linkage to 8q24 in a European family with familial adult myoclonic epilepsy (FAME). Neurology 2002; 58:941-944.
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