학술논문

Polymicrogyria-associated epilepsy: a multicenter phenotypic study from the Epilepsy Phenome/Genome Project.
Document Type
article
Source
Epilepsia. 54(8)
Subject
EPGP Investigators
Cerebral Cortex
Humans
Epilepsy
Magnetic Resonance Imaging
Electroencephalography
Retrospective Studies
Cohort Studies
Age of Onset
Phenotype
Adolescent
Adult
Middle Aged
Child
Child
Preschool
Infant
Female
Male
Functional Laterality
Malformations of Cortical Development
Young Adult
Epilepsy Phenome/Genome Project
Perisylvian
Polymicrogyria
Neurosciences
Neurodegenerative
Pediatric
Brain Disorders
Clinical Research
2.1 Biological and endogenous factors
Aetiology
Neurological
Epilepsy Phenome
Genome Project
Clinical Sciences
Neurology & Neurosurgery
Language
Abstract
PurposePolymicrogyria (PMG) is an epileptogenic malformation of cortical development. We describe the clinical epilepsy and imaging features of a large cohort with PMG-related epilepsy.MethodsParticipants were recruited through the Epilepsy Phenome/Genome Project, a multicenter collaborative effort to collect detailed phenotypic data on individuals with epilepsy. We reviewed phenotypic data from participants with epilepsy and PMG.Key findingsWe identified 87 participants, 43 female and 44 male, with PMG and epilepsy. Median age of seizure onset was 3 years (range