What does spinocerebellar degenerations mean?
Definitions for spinocerebellar degenerations
spinocere·bel·lar degen·er·a·tions
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Wikipedia
spinocerebellar degenerations
Spinocerebellar ataxia (SCA) is a progressive, degenerative, genetic disease with multiple types, each of which could be considered a neurological condition in its own right. An estimated 150,000 people in the United States have a diagnosis of spinocerebellar ataxia at any given time. SCA is hereditary, progressive, degenerative, and often fatal. There is no known effective treatment or cure. SCA can affect anyone of any age. The disease is caused by either a recessive or dominant gene. In many cases people are not aware that they carry a relevant gene until they have children who begin to show signs of having the disorder.
U.S. National Library of Medicine
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.
Numerology
Chaldean Numerology
The numerical value of spinocerebellar degenerations in Chaldean Numerology is: 6
Pythagorean Numerology
The numerical value of spinocerebellar degenerations in Pythagorean Numerology is: 2
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"spinocerebellar degenerations." Definitions.net. STANDS4 LLC, 2024. Web. 24 Apr. 2024. <https://www.definitions.net/definition/spinocerebellar+degenerations>.
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