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Article

Autosomal dominant epilepsy with auditory features: a new LGI1 family including a phenocopy with cortical dysplasia.

Journal of neurology - 1 Jan 2016

Klein Karl Martin, Pendziwiat Manuela, Cohen Rony, Appenzeller Silke, de Kovel Carolien G F, Rosenow Felix, Koeleman Bobby P C, Kuhlenbäumer Gregor, Sheintuch Liron, Veksler Ronel, Friedman Alon, Afawi Zaid, Helbig Ingo

Abstract excerpt

We report a new family with autosomal dominant epilepsy with auditory features (ADEAF) including focal cortical dysplasia (FCD) in the proband. We aim to identify the molecular cause in this family and clarify the relationship between FCD and ADEAF. A large Iranian Jewish family including 14 individuals with epileptic seizures was phenotyped including high-resolution 3-T MRI. We performed linkage analysis and...

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Electroencephalography
Epilepsy, Frontal Lobe
Iran
Israel
Jews

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Malformations of Cortical Development

Sleep Wake Disorders

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Identifiers

PMID: 26459092
DOI: 10.1007/s00415-015-7921-2

Genes

LGI1
RELN

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

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