Epilessia ed anomalie epilettiformi EEG in una casistica di pazienti affette da Sindrome di Rett

G. Barcia; G. G. Salerno; S. Sangiorgi; A. Posar; M. C. Scaduto; G. Ambrosetto; A. Arbizzani; M. Santucci

Epilessia ed anomalie epilettiformi EEG in una casistica di pazienti affette da Sindrome di Rett

Translated title of the contribution: Epilepsy and EEG abnormalities in a series of patients affected by Rett Syndrome

G. Barcia, G. G. Salerno, S. Sangiorgi, A. Posar, M. C. Scaduto, G. Ambrosetto, A. Arbizzani, M. Santucci

Istituto Scienze Neurologiche

Research output: Contribution to journal › Article › peer-review

Abstract

Rett Syndrome (RS) is a neurodevelopmental disorder mainly affecting females,mostly linked to MECP2 gene mutations. EEG abnormalities and epilepsy are frequent in RS. The authors refer on clinical and EEG data of 16 patients affected by classical RS. The epilepsy was observed in 11 subjects. We analyze the main features of epilepsy and EEG in order to evaluate correlations between clinical stages, epilepsy and EEG evolution.

Translated title of the contribution	Epilepsy and EEG abnormalities in a series of patients affected by Rett Syndrome
Original language	Italian
Pages (from-to)	93-95
Number of pages	3
Journal	Bollettino - Lega Italiana contro l'Epilessia
Issue number	138
Publication status	Published - 2008

ASJC Scopus subject areas

Clinical Neurology

Cite this

@article{87de658ab06340d1bfa269a018cb40d8,

title = "Epilessia ed anomalie epilettiformi EEG in una casistica di pazienti affette da Sindrome di Rett",

abstract = "Rett Syndrome (RS) is a neurodevelopmental disorder mainly affecting females,mostly linked to MECP2 gene mutations. EEG abnormalities and epilepsy are frequent in RS. The authors refer on clinical and EEG data of 16 patients affected by classical RS. The epilepsy was observed in 11 subjects. We analyze the main features of epilepsy and EEG in order to evaluate correlations between clinical stages, epilepsy and EEG evolution.",

keywords = "EEG abnormalities, Epilepsy, Rett Syndrome",

author = "G. Barcia and Salerno, {G. G.} and S. Sangiorgi and A. Posar and Scaduto, {M. C.} and G. Ambrosetto and A. Arbizzani and M. Santucci",

year = "2008",

language = "Italian",

pages = "93--95",

journal = "Bollettino - Lega Italiana contro l'Epilessia",

issn = "0394-560X",

publisher = "Lega Italiana contro l'Epilessia",

number = "138",

}

TY - JOUR

T1 - Epilessia ed anomalie epilettiformi EEG in una casistica di pazienti affette da Sindrome di Rett

AU - Barcia, G.

AU - Salerno, G. G.

AU - Sangiorgi, S.

AU - Posar, A.

AU - Scaduto, M. C.

AU - Ambrosetto, G.

AU - Arbizzani, A.

AU - Santucci, M.

PY - 2008

Y1 - 2008

N2 - Rett Syndrome (RS) is a neurodevelopmental disorder mainly affecting females,mostly linked to MECP2 gene mutations. EEG abnormalities and epilepsy are frequent in RS. The authors refer on clinical and EEG data of 16 patients affected by classical RS. The epilepsy was observed in 11 subjects. We analyze the main features of epilepsy and EEG in order to evaluate correlations between clinical stages, epilepsy and EEG evolution.

AB - Rett Syndrome (RS) is a neurodevelopmental disorder mainly affecting females,mostly linked to MECP2 gene mutations. EEG abnormalities and epilepsy are frequent in RS. The authors refer on clinical and EEG data of 16 patients affected by classical RS. The epilepsy was observed in 11 subjects. We analyze the main features of epilepsy and EEG in order to evaluate correlations between clinical stages, epilepsy and EEG evolution.

KW - EEG abnormalities

KW - Epilepsy

KW - Rett Syndrome

UR - http://www.scopus.com/inward/record.url?scp=77953093718&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=77953093718&partnerID=8YFLogxK

M3 - Articolo

AN - SCOPUS:77953093718

SP - 93

EP - 95

JO - Bollettino - Lega Italiana contro l'Epilessia

JF - Bollettino - Lega Italiana contro l'Epilessia

SN - 0394-560X

IS - 138

ER -

Epilessia ed anomalie epilettiformi EEG in una casistica di pazienti affette da Sindrome di Rett

Abstract

ASJC Scopus subject areas

Other files and links

Fingerprint

Cite this