Introduction Dravet Syndrome, initially known as Severe Myoclonic Epilepsy of Infancy (SMEI), is a rare and catastrophic form of intractable epilepsy
Abstract Rasmussen’s Encephalitis (RE) is a rare, progressive neurological disorder, predominantly affecting the pediatric population. Characterized by unilateral hemispheric inflammation, recurrent
Introduction Prader-Willi Syndrome (PWS) is a complex genetic disorder caused by the loss of function of specific genes in chromosome 15.
Abstract Ohtahara Syndrome is a rare and severe form of epilepsy that manifests in early infancy. This review aims to explore
Date: Abstract Neuronal Ceroid Lipofuscinoses (NCLs) represent a group of rare, inherited, progressive neurodegenerative disorders primarily affecting children. This extensive review
Abstract:This article provides an in-depth review of epilepsy in children, delving into its etiological factors, clinical presentation, diagnostic modalities, and therapeutic
Abstract Landau-Kleffner Syndrome (LKS) is a rare neurological disorder, primarily affecting children, and characterized by acquired aphasia and epileptic seizures. This
Abstract: This article explores the spectrum of pediatric neurological pathologies associated with maternal alcohol consumption during pregnancy. It emphasizes the clinical