Epileptic Disorders
MENUAutosomal dominant lateral temporal lobe epilepsy associated with a novel reelin mutation Volume 22, numéro 4, August 2020
Auteurs
Aims
1 IRCCS-Istituto delle Scienze Neurologiche di Bologna, Unit of Neurology, Bellaria Hospital, Bologna, Italy
2 CNR-Neuroscience Institute, Section of Padua, Padova, Italy
3 IRCCS-Istituto delle Scienze Neurologiche di Bologna, Unit of Neurological Clinic, Bellaria Hospital, Bologna, Italy
4 IRCCS-Istituto delle Scienze Neurologiche di Bologna, Unit of Neuroradiology, Bellaria Hospital, Bologna, Italy
5 Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy
6 Department of Biomedical Sciences, University of Padua, Padova, Italy
* Correspondence: Roberto Michelucci
IRCCS-Istituto delle Scienze Neurologiche di Bologna,
Unit of Neurology, Bellaria Hospital,
Via Altura 3 40139 Bologna, Italy
- Mots-clés : autosomal dominant lateral temporal lobe epilepsy, autosomal dominant epilepsy with auditory features, reelin, lateral temporal lobe seizures
- DOI : 10.1684/epd.2020.1176
- Page(s) : 443-8
- Année de parution : 2020
Reelin mutations are responsible for a minority of families with autosomal dominant lateral temporal lobe epilepsy. Here, we report a novel nuclear family with distinct clinical and neuroradiological findings.