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Panayiotopoulos syndrome: a consensus view

Published online by Cambridge University Press:  17 February 2006

Colin Ferrie
Affiliation:
Department of Paediatric Neurology, Leeds General Infirmary, UK.
Roberto Caraballo
Affiliation:
Servicio de Neurologia, Hospital de Ninos Prof Dr JP Garrahan, Buenos Aires, Argentina.
Athanasios Covanis
Affiliation:
Neurology Department, The Children's Hospital Agia Sophia, Athens, Greece.
Veysi Demirbilek
Affiliation:
Cerrah Pasa Medical Faculty, Department of Neurology, Istanbul University, Turkey.
Aysin Dervent
Affiliation:
Cerrah Pasa Medical Faculty, Department of Neurology, Istanbul University, Turkey.
Sara Kivity
Affiliation:
Pediatric Epilepsy Unit and EEG Laboratory, Schneider Children's Medical Centre of Israel, Petach, Tiqwa, Israel.
Michael Koutroumanidis
Affiliation:
Department of Clinical Neurophysiology and Epilepsies, St Thomas' Hospital, London, UK.
Zarko Martinovic
Affiliation:
Department of Epilepsy and Clinical Neurosciences, Belgrade University Medical School, Serbia and Montenegro.
Hirokazu Oguni
Affiliation:
Department of Pediatrics, Tokyo Women's Medical University, Japan.
Alberto Verrotti
Affiliation:
Division of Pediatrics, Department of Medicine, Ospedale Policlinico, Chieti, Italy.
Federico Vigevano
Affiliation:
Division of Neurology, Bambino Gesu Children Hospital, Rome, Italy.
Kazuyoshi Watanabe
Affiliation:
Department of Pediatrics, Nagoya University School of Medicine, Nagoya, Japan.
Despina Yalcin
Affiliation:
Neurological Clinic, Sisli Etfal Education Hospital, Istanbul, Turkey.
Harami Yoshinaga
Affiliation:
Department of Child Neurology, Okayama University Medical School, Japan.
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Abstract

The aim of this paper is to promote the correct classification of, and provide guidelines on, the diagnosis and management of Panayiotopoulos syndrome (PS). An international consortium of established researchers in the field collaborated to produce a consensus document. The resulting document defines PS, characterizes its electro-clinical features, considers its likely pathogenesis, and provides guidance on appropriate management. We conclude that PS is a common idiopathic, benign seizure disorder of childhood, which should be classified as an autonomic epilepsy, rather than an occipital epilepsy.

Type
Review
Copyright
2006 Mac Keith Press

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