Mesial temporal lobe epilepsy associated with KCNT1 mutation

Seizure. 2017 Feb:45:181-183. doi: 10.1016/j.seizure.2016.12.018. Epub 2016 Dec 26.

Authors

N Hansen¹, G Widman², E Hattingen³, C E Elger², W S Kunz²

Affiliations

¹ Department of Epileptology, University of Bonn, Sigmund Freud Str. 25, 53127 Bonn, Germany. Electronic address: Niels.Hansen@ukb.uni-bonn.de.
² Department of Epileptology, University of Bonn, Sigmund Freud Str. 25, 53127 Bonn, Germany.
³ Department of Neuroradiology, University of Bonn, Sigmund Freud Str. 25, 53127 Bonn, Germany.

PMID: 28081520
DOI: 10.1016/j.seizure.2016.12.018

No abstract available

Publication types

Case Reports
Video-Audio Media

MeSH terms

Adult
Brain / diagnostic imaging
Cerebellar Ataxia / diagnostic imaging
Cerebellar Ataxia / drug therapy
Cerebellar Ataxia / genetics
Cerebellar Ataxia / physiopathology
Epilepsy, Temporal Lobe / diagnostic imaging
Epilepsy, Temporal Lobe / drug therapy
Epilepsy, Temporal Lobe / genetics*
Epilepsy, Temporal Lobe / physiopathology
Female
Humans
Intellectual Disability / diagnostic imaging
Intellectual Disability / drug therapy
Intellectual Disability / genetics
Intellectual Disability / physiopathology
Male
Mutation*
Nerve Tissue Proteins / genetics*
Phenotype
Potassium Channels / genetics*
Potassium Channels, Sodium-Activated
Siblings

Substances

KCNT1 protein, human
Nerve Tissue Proteins
Potassium Channels
Potassium Channels, Sodium-Activated