Introduction Prader-Willi Syndrome (PWS) is a complex genetic disorder caused by the loss of function of specific genes in chromosome 15.
Abstract Narcolepsy Type 1, a rare sleep disorder characterized by excessive daytime sleepiness and cataplexy, presents a unique challenge in sleep
Introduction Neuromyelitis Optica (NMO), also known as Devic’s disease, is a rare, autoimmune disorder primarily affecting the spinal cord and optic
Abstract Corticobasal Degeneration (CBD) is a rare, progressive neurodegenerative disorder. This review delves into its neuropathological hallmarks, clinical manifestations, diagnostic challenges,
Abstract: This article delves into the multifaceted health consequences of pesticide exposure through food consumption, examining the biochemical pathways, clinical manifestations,
Abstract: Unveiling a Persistent Cephalic Phenomenon The Sudden Onset Conundrum: NDPH’s Clinical Signature New Daily Persistent Headache (NDPH) presents as a
Abstract: The Pharmacological Balancing Act The Dichotomy of Seizure Suppression Anticonvulsant medications, cornerstone agents in the management of epilepsy, come with
Introduction Cervical Dystonia, also known as spasmodic torticollis, is a focal dystonia characterized by involuntary muscle contractions in the neck. This
Abstract: Chronic headache, encompassing various subtypes like chronic migraine, tension-type headache, and cluster headache, poses significant management challenges. This review elucidates
Abstract Creutzfeldt-Jakob Disease (CJD) is a rare and fatal prion disease that affects the brain. This review aims to dissect the