Myoclonus epilepsy and ataxia due to potassium channel mutation (MEAK): a cause of progressive myoclonic epilepsy

Acta Neurol Belg. 2022 Jun;122(3):801-803. doi: 10.1007/s13760-021-01645-x. Epub 2021 Mar 16.

Authors

Rohan R Mahale¹, Ravindu Tiwari², Gautham Arunachal³, Hansashree Padmanabha², Pooja Mailankody²

Affiliations

¹ Department of Neurology, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, Karnataka, 560029, India. rohanmahale83@gmail.com.
² Department of Neurology, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, Karnataka, 560029, India.
³ Department of Human Genetics, NIMHANS, Bangalore, India.

PMID: 33725338
DOI: 10.1007/s13760-021-01645-x

No abstract available

Keywords: Ataxia; KCNC1 gene; Myoclonus; Progressive myoclonic epilepsy.

Publication types

Letter

MeSH terms

Ataxia / genetics
Epilepsies, Myoclonic*
Humans
Mutation / genetics
Myoclonic Epilepsies, Progressive* / genetics
Myoclonus*
Potassium Channels / genetics

Substances

Potassium Channels