Abstract Alexander Disease (AD) is a rare, progressive neurodegenerative disorder, primarily affecting the white matter of the brain. This comprehensive review
Abstract Vanishing White Matter Disease (VWM) is a rare, progressive leukodystrophy characterized by demyelination and neurodegeneration. This comprehensive review seeks to
Abstract: The Confluence of Genetics and Blood Pressure The Hypertensive Heritage: A Genetic Perspective Hypertension, a cardinal risk factor for cardiovascular
Date: Abstract Neuronal Ceroid Lipofuscinoses (NCLs) represent a group of rare, inherited, progressive neurodegenerative disorders primarily affecting children. This extensive review
Abstract: Demyelinating disorders represent a heterogeneous group of neurological conditions characterized by the damage to the myelin sheath of neurons. This
Abstract Perry Syndrome is a rare, progressive neurodegenerative disorder characterized by Parkinsonism, depression, weight loss, and hypoventilation. This review provides an
Abstract Pantothenate Kinase-Associated Neurodegeneration (PKAN) is a rare, inherited neurodegenerative disorder characterized by iron accumulation in the brain. This extensive review
Abstract Canavan Disease is a rare, inherited neurodegenerative disorder characterized by white matter deterioration in the brain. This exhaustive review delves
Abstract Refsum Disease is a rare genetic disorder characterized by the accumulation of phytanic acid in the body, leading to a
Abstract Machado-Joseph Disease (MJD), also known as Spinocerebellar Ataxia Type 3, is a rare, inherited neurodegenerative disorder. This extensive review seeks