What does spinocerebellar ataxias mean?

Definitions for spinocerebellar ataxias
spinocere·bel·lar atax·i·as

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Wikipedia

  1. spinocerebellar ataxias

    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

  1. Spinocerebellar Ataxias

    A group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)

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Numerology

  1. Chaldean Numerology

    The numerical value of spinocerebellar ataxias in Chaldean Numerology is: 8

  2. Pythagorean Numerology

    The numerical value of spinocerebellar ataxias in Pythagorean Numerology is: 4

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