Abstract Whipple’s Disease is a rare multisystemic disorder caused by the bacterium Tropheryma whipplei, which can lead to significant central nervous
Convergence Insufficiency: The Strain of Alignment Convergence insufficiency (CI), a prevalent binocular vision disorder, is marked by a decreased ability to
Abstract CADASIL is a genetic vascular disorder characterized by recurrent ischemic strokes and progressive subcortical vascular dementia. This thorough review scrutinizes
Abstract Dentatorubral-Pallidoluysian Atrophy (DRPLA) is a rare, heritable neurodegenerative disorder characterized by ataxia, choreoathetosis, seizures, and cognitive deterioration. This review provides
Introduction Kufs Disease, a phenotype of Neuronal Ceroid Lipofuscinosis (NCL), presents as an autosomal recessive neurodegenerative disorder, predominantly afflicting adults. It
Genetic Harbingers: Inherited Predispositions to Neoplastic Growth Chromosomal Custodians and Genetic Syndromes In the realm of cerebral oncogenesis, genetic constitution forms
Abstract: Alzheimer’s disease, a devastating neurodegenerative disorder, has long been the focus of extensive research aimed at understanding its intricate origins.
Abstract Hereditary Spastic Paraplegia (HSP) represents a heterogeneous group of inherited disorders characterized by progressive lower extremity spasticity and weakness. This
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