Autosomal recessive cortical myoclonic tremor and epilepsy
Evidence-based neurology checklist on autosomal recessive cortical myoclonic tremor and epilepsy: Genetics This is caused by mutations in the CNTN2 gene Clinical features Treatment Investigations
Genetics
- This is caused by mutations in the CNTN2 gene
Clinical features
Treatment
Investigations
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.
- Striano P, Zara F, Striano S, Minetti C. Autosomal recessive epilepsy associated with contactin 2 mutation is different from familial cortical tremor, myoclonus and epilepsy. Brain 2013; 136:e253.
