Dentatorubral-Pallidoluysian Atrophy (DRPLA): A Critical Review of Its Genetic Origins, Neuropathological Progression, and Clinical Management
Abstract Dentatorubral-Pallidoluysian Atrophy (DRPLA) is a rare, heritable neurodegenerative disorder characterized by ataxia, choreoathetosis, seizures, and cognitive deterioration. This review provides