We report three nuclear families in which affected individuals had the onset during childhood or adolescence of drug-responsive focal seizures characterized by prominent vertiginous auras. The interictal EEG abnormalities were localized around the parieto-temporo-occipital regions and MRI was normal. Genetic analysis excluded epitempin mutations. We propose the existence of a familial focal epilepsy characterized by prominent vertiginous auras suggesting a parietal or parieto-temporal onset.

Familial focal epilepsy with vertiginous aura: A new entity?|Epilessia focale familiare con sintomi vertiginosi: Una nuova forma di epilessia focale ereditaria?

Nobile C
2005

Abstract

We report three nuclear families in which affected individuals had the onset during childhood or adolescence of drug-responsive focal seizures characterized by prominent vertiginous auras. The interictal EEG abnormalities were localized around the parieto-temporo-occipital regions and MRI was normal. Genetic analysis excluded epitempin mutations. We propose the existence of a familial focal epilepsy characterized by prominent vertiginous auras suggesting a parietal or parieto-temporal onset.
2005
Familial focal epilepsy
LGI1/Epitempin gene
Parietal lobe epilepsy
Vertiginous symptoms
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/308064
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