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Spinocerebellar Degenerations

More information in Books or onNLM PubMed
Definition: 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.     
Examples Friedreich Ataxia; Myoclonic Cerebellar Dyssynergia; Olivopontocerebellar Atrophies; Spinocerebellar Ataxias 		Other names Syndrome, Marinesco-Sjogren; Spinocerebellar Disease; Spinocerebellar Degenerations, Inherited; Spinocerebellar Degenerations, Hereditary; Spinocerebellar Degenerations, Familial; Spinocerebellar Degeneration, Inherited; Spinocerebellar Degeneration, Hereditary; Spinocerebellar Degeneration, Familial; Spino-Cerebellar Degeneration; Spino Cerebellar Degeneration; Primary Cerebellar Degenerations; Primary Cerebellar Degeneration; Marinesco Sjogren Syndrome; Maries Cerebellar Ataxia; Inherited Spinocerebellar Degeneration; Hereditary Spinocerebellar Degeneration; Hereditary Ataxias; Hereditary Ataxia; Familial Spinocerebellar Degeneration; Degenerations, Spinocerebellar
 
SubstanceCAS Registry & nameCategoriesSource
Spinocerebellar ataxia 22  0   *Spinocerebellar Degenerations.
Spinocerebellar ataxia, X-linked, 4  0   *Spinocerebellar Degenerations.
Spinocerebellar ataxia, X-linked, 2  0   *Spinocerebellar Degenerations.
Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy  0   *Spinocerebellar Degenerations.
Spinocerebellar ataxia, autosomal recessive 6  0   *Spinocerebellar Degenerations.
Spinocerebellar ataxia, autosomal recessive 5  0   *Spinocerebellar Degenerations.
Spinocerebellar ataxia, autosomal recessive 4  0   *Spinocerebellar Degenerations.
Spinocerebellar ataxia, autosomal recessive 3  0   *Spinocerebellar Degenerations.
Spinocerebellar ataxia, autosomal recessive 1  0   *Spinocerebellar Degenerations.
Spinocerebellar ataxia 8  0   *Spinocerebellar Degenerations.
Spinocerebellar ataxia 30  0   *Spinocerebellar Degenerations.
Spinocerebellar ataxia 28  0   *Spinocerebellar Degenerations.
Spinocerebellar ataxia 27  0   *Spinocerebellar Degenerations.
Spinocerebellar ataxia 23  0   *Spinocerebellar Degenerations.
Spinocerebellar ataxia 21  0   *Spinocerebellar Degenerations.
Spinocerebellar ataxia 19  0   *Spinocerebellar Degenerations.
Sensorimotor neuropathy with ataxia, autosomal dominant  0   *Spinocerebellar Degenerations.
Spinocerebellar ataxia 14  0   *Spinocerebellar Degenerations.
Spinocerebellar ataxia 13  0   *Spinocerebellar Degenerations.
Mousa Al din Al Nassar syndrome  0   *Abnormalities, Multiple *Cataract *Corneal Dystrophies, Hereditary *Myopia *Spinocerebellar Degenerations.
Posterior column ataxia  0   *Sensation Disorders *Spinocerebellar Degenerations.
Infantile onset spinocerebellar ataxia  0   *Spinocerebellar Degenerations.
Corneal cerebellar syndrome  0   *Corneal Dystrophies, Hereditary *Spinocerebellar Degenerations.
SCA8 protein, mouse  0   *Nerve Tissue Proteins Spinocerebellar Degenerations. Brain Res 2008 Oct 3;1233():176-84
Hereditary spinal ataxia  0   *Spinocerebellar Degenerations/congenital.
ATXN8OS gene product, human  0   *Nerve Tissue Proteins *RNA, Untranslated Spinocerebellar Degenerations. Hum Mol Genet. 2000 Sep 1;9(14):2125-30
ataxin-7  0   *Nerve Tissue Proteins Spinocerebellar Degenerations Protein Isoforms. Nat Genet 1997 Sep;17(1):65-70
SCA2 protein  0   *Nerve Tissue Proteins Spinocerebellar Degenerations. Nat Genet 1996 Nov;14(3):269-76

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Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012
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