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DeCS
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Descriptor English:
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Spinocerebellar Ataxias
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Descriptor Spanish:
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Ataxias Espinocerebelosas
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Descriptor Portuguese:
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Ataxias Espinocerebelares
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Synonyms English:
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Spinocerebellar Ataxia Type 1
Spinocerebellar Ataxia Type 2
Spinocerebellar Ataxia Type 4
Spinocerebellar Ataxia Type 5
Spinocerebellar Ataxia Type 6
Spinocerebellar Ataxia Type 7
Spinocerebellar Atrophies
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Tree Number:
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C10.228.140.252.190.530
C10.228.140.252.700.700
C10.228.854.787.875
C10.574.500.825.700
C10.597.350.090.500.530
C16.320.400.780.875
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Definition English:
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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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Indexing Annotation English:
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SPINOCEREBELLAR ATAXIA TYPE 3 see MACHADO-JOSEPH DISEASE is available
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See Related English:
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Ataxin-1
Ataxin-2
Ataxin-3
Ataxin-7
Ataxins
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History Note English:
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2000; use SPINOCEREBELLAR DEGENERATION 1987-1999
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Allowable Qualifiers English:
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Record Number:
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34243
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Unique Identifier:
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D020754
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Occurrence in VHL:
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Similar:
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DeCS CID-10 SciELO LILACS LIS
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