John Libbey Eurotext

Autosomal dominant lateral temporal lobe epilepsy associated with a novel reelin mutation Volume 22, issue 4, August 2020

Figures

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Authors
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

Aims

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.