Prevalence and genotypic associations of epilepsy in Prader-Willi Syndrome: A systematic review and meta-analysis

•The prevalence of epilepsy in Prader-Willi syndrome was 11% and the prevalence of febrile seizures was 9%.•Deletions in the 15q11-q13 region increased the likelihood of febrile seizures by 3.76-fold compared with chromosome 15 disomies.•Although there is an deleterious trend for deletions in epilep...

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Veröffentlicht in:	Epilepsy & behavior 2024-06, Vol.155, p.109803-109803, Article 109803
Hauptverfasser:	Pascual-Morena, Carlos, Martínez-Vizcaíno, Vicente, Cavero-Redondo, Iván, Álvarez-Bueno, Celia, Martínez-García, Irene, Rodríguez-Gutiérrez, Eva, Otero-Luis, Iris, del Saz-Lara, Andrea, Saz-Lara, Alicia
Format:	Artikel
Sprache:	eng
Schlagworte:	Chromosomes, Human, Pair 15 - genetics Epidemiology Epilepsy - epidemiology Epilepsy - genetics Genetic Genotype Humans Neuroepidemiology Neurology Prader-Willi Syndrome - complications Prader-Willi Syndrome - epidemiology Prader-Willi Syndrome - genetics Prevalence Rare disease
Online-Zugang:	Volltext
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