Cerebellar hypoplasia is the underdevelopment of the cerebellum. Symptoms can include seizures, developmental delays, and difficulties with movement. Cerebellar hypoplasia is the underdevelopment of a ...

Cerebellar rhythm loss due to climbing fiber regression is a shared pathophysiology of motor deficits across cerebellar ataxias. Cerebellar ataxias are a group of genetic and non-genetic disorders ...

Background Multiple system atrophy (MSA) is a progressive neurodegenerative disorder of unknown etiology, manifesting as combination of parkinsonism, cerebellar syndrome and dysautonomia.

Spinal muscular atrophy is a rare genetic disease of the nerve cells in the spinal cord that can appear as early as infancy. The disease leads to a progressive loss of muscle strength. Those affected ...