Spinocerebellar Degenerations |
| Early Onset Cerebellar Ataxia; Familial Spinocerebellar Degenerations; Hereditary Spinocerebellar Degenerations; Inherited Spinocerebellar Degenerations; Late Onset Cerebellar Ataxia; Marie's Cerebellar Ataxia; Spino Cerebellar Degenerations |
| A heterogenous group of degenerative syndromes marked by progressive cerebellar dysfunction either in isolation or combined with other neurologic manifestations. Sporadic and inherited subtypes occur. Inheritance patterns include autosomal dominant, autosomal recessive, and X-linked. |
|
|
|