Cerebral atherosclerosis Cerebral atherosclerosis also called cerebral arteriosclerosis, is the result of thickening and hardening of the walls of the arteries in the brain. Symptoms
Corticobasal degeneration Corticobasal degeneration is a rare progressive neurological disorder characterized by nerve cell loss and atrophy (shrinkage) of multiple areas of the brain including
Brody myopathy Brody myopathy also called Brody disease, is a rare hereditary condition that affects the skeletal muscles, which are the muscles used for movement. Affected
Alternating hemiplegia of childhood Alternating hemiplegia of childhood is a neurological condition that usually affects children before 18 months of age that is characterized by
Wolman disease Wolman disease is a congenital disease characterized by an impaired metabolism of the fats (lipids). Wolman disease is the most severe type of
Werdnig Hoffmann disease Werdnig Hoffmann disease is now called spinal muscular atrophy type 1 or severe infantile spinal muscular atrophy, is a genetic neuromuscular disorder
Akinetopsia Akinetopsia also known as cerebral akinetopsia or motion blindness, is a rare neuropsychological disorder in which a patient specifically loses the ability to perceive visual motion despite