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Panayiotopoulos syndrome: Difference between revisions
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'''Panayiotopoulos syndrome''' is a common idiopathic childhood-related seizure disorder that occurs exclusively in otherwise normal children (idiopathic epilepsy) and manifests mainly with autonomic [[epilepsy|epileptic seizures]] and autonomic [[status epilepticus]]. An expert consensus has defined [[Chrysostomos P. Panayiotopoulos|Panayiotopoulos]] syndrome as "a benign age-related focal seizure disorder occurring in early and mid-childhood. It is characterized by seizures, often prolonged, with predominantly autonomic symptoms, and by an [[electroencephalogram|EEG]] that shows shifting and/or multiple foci, often with occipital predominance<ref>[https://en.wikipedia.org/w/index.php?title=Panayiotopoulos_syndrome&oldid=656785900 wikipedia:Panayiotopoulos syndrome]</ref> | '''Panayiotopoulos syndrome''' is a common idiopathic childhood-related seizure disorder that occurs exclusively in otherwise normal children (idiopathic epilepsy) and manifests mainly with autonomic [[epilepsy|epileptic seizures]] and autonomic [[status epilepticus]]. An expert consensus has defined [[Chrysostomos P. Panayiotopoulos|Panayiotopoulos]] syndrome as "a benign age-related focal seizure disorder occurring in early and mid-childhood. It is characterized by seizures, often prolonged, with predominantly autonomic symptoms, and by an [[electroencephalogram|EEG]] that shows shifting and/or multiple foci, often with occipital predominance<ref>[https://en.wikipedia.org/w/index.php?title=Panayiotopoulos_syndrome&oldid=656785900 wikipedia:Panayiotopoulos syndrome]</ref> | ||
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[[Category:Neurological disorder]] | [[Category:Neurological disorder]] | ||
Revision as of 18:55, 19 October 2015
Panayiotopoulos syndrome is a common idiopathic childhood-related seizure disorder that occurs exclusively in otherwise normal children (idiopathic epilepsy) and manifests mainly with autonomic epileptic seizures and autonomic status epilepticus. An expert consensus has defined Panayiotopoulos syndrome as "a benign age-related focal seizure disorder occurring in early and mid-childhood. It is characterized by seizures, often prolonged, with predominantly autonomic symptoms, and by an EEG that shows shifting and/or multiple foci, often with occipital predominance[1]
