Other terms
Spino Cerebellar Degenerations,Degeneration, Spino Cerebellar,Degenerations, Spino Cerebellar,Spino Cerebellar Degeneration,Spinocerebellar Diseases,Spinocerebellar Disease,Spinocerebellar Degeneration,Degeneration, Spinocerebellar,Degenerations, Spinocerebellar,Spino-Cerebellar Degenerations,Degeneration, Spino-Cerebellar,Degenerations, Spino-Cerebellar,Spino-Cerebellar Degeneration,Cerebellar Ataxia, Early Onset,Early Onset Cerebellar Ataxia,Marinesco-Sjogren Syndrome,Marinesco Sjogren Syndrome,Syndrome, Marinesco-Sjogren,Cerebellar Degenerations, Primary,Cerebellar Degeneration, Primary,Degeneration, Primary Cerebellar,Degenerations, Primary Cerebellar,Primary Cerebellar Degeneration,Primary Cerebellar Degenerations,Corticostriatal-Spinal Degeneration,Corticostriatal Spinal Degeneration,Corticostriatal-Spinal Degenerations,Degeneration, Corticostriatal-Spinal,Degenerations, Corticostriatal-Spinal,Marie Cerebellar Ataxia,Cerebellar Ataxia, Marie,Marie's Cerebellar Ataxia,Cerebellar Ataxia, Marie's,Maries Cerebellar Ataxia,Ataxias, Hereditary,Ataxia, Hereditary,Hereditary Ataxia,Hereditary Ataxias,Hereditary Spinocerebellar Degenerations,Degeneration, Hereditary Spinocerebellar,Degenerations, Hereditary Spinocerebellar,Hereditary Spinocerebellar Degeneration,Spinocerebellar Degeneration, Hereditary,Spinocerebellar Degenerations, Hereditary,Inherited Spinocerebellar Degenerations,Degeneration, Inherited Spinocerebellar,Degenerations, Inherited Spinocerebellar,Inherited Spinocerebellar Degeneration,Spinocerebellar Degeneration, Inherited,Spinocerebellar Degenerations, Inherited,Familial Spinocerebellar Degenerations,Degeneration, Familial Spinocerebellar,Degenerations, Familial Spinocerebellar,Familial Spinocerebellar Degeneration,Spinocerebellar Degeneration, Familial,Spinocerebellar Degenerations, Familial,Cerebellar Ataxia, Late Onset,Late Onset Cerebellar Ataxia
Description
Spinocerebellar 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.
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