Epilessia focale familiare con sintomi vertiginosi: Una nuova forma di epilessia focale ereditaria?

R. Michelucci; P. Striano; S. Testoni; S. Striano; P. Ruosi; L. Volpi; G. Rubboli; P. Riguzzi; C. A. Tassinari; C. Nobile

Epilessia focale familiare con sintomi vertiginosi: Una nuova forma di epilessia focale ereditaria?

Translated title of the contribution: Familial focal epilepsy with vertiginous aura: A new entity?

R. Michelucci, P. Striano, S. Testoni, S. Striano, P. Ruosi, L. Volpi, G. Rubboli, P. Riguzzi, C. A. Tassinari, C. Nobile

Research output: Contribution to journal › Article

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.

Original language	Italian
Pages (from-to)	79-80
Number of pages	2
Journal	Bollettino - Lega Italiana contro l'Epilessia
Issue number	129-130
Publication status	Published - 2005

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ASJC Scopus subject areas

Clinical Neurology

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Michelucci, R., Striano, P., Testoni, S., Striano, S., Ruosi, P., Volpi, L., Rubboli, G., Riguzzi, P., Tassinari, C. A., & Nobile, C. (2005). Epilessia focale familiare con sintomi vertiginosi: Una nuova forma di epilessia focale ereditaria? Bollettino - Lega Italiana contro l'Epilessia, (129-130), 79-80.

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title = "Epilessia focale familiare con sintomi vertiginosi: Una nuova forma di epilessia focale ereditaria?",

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.",

keywords = "Familial focal epilepsy, LGI1/Epitempin gene, Parietal lobe epilepsy, Vertiginous symptoms",

author = "R. Michelucci and P. Striano and S. Testoni and S. Striano and P. Ruosi and L. Volpi and G. Rubboli and P. Riguzzi and Tassinari, {C. A.} and C. Nobile",

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T1 - Epilessia focale familiare con sintomi vertiginosi

T2 - Una nuova forma di epilessia focale ereditaria?

AU - Michelucci, R.

AU - Striano, P.

AU - Testoni, S.

AU - Striano, S.

AU - Ruosi, P.

AU - Volpi, L.

AU - Rubboli, G.

AU - Riguzzi, P.

AU - Tassinari, C. A.

AU - Nobile, C.

PY - 2005

Y1 - 2005

N2 - 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.

AB - 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.

KW - Familial focal epilepsy

KW - LGI1/Epitempin gene

KW - Parietal lobe epilepsy

KW - Vertiginous symptoms

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JO - Bollettino - Lega Italiana contro l'Epilessia

JF - Bollettino - Lega Italiana contro l'Epilessia

SN - 0394-560X

IS - 129-130

ER -

Epilessia focale familiare con sintomi vertiginosi: Una nuova forma di epilessia focale ereditaria?

Abstract

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