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ataxie spinocerebelárne

  1. Record numberd020754
    Date06.06.2025
    TypeM - MESH
    Topical termataxie spinocerebelárne
    Other termEnglish (Pseudonym) Spinocerebellar Ataxia Type 1
    English (Pseudonym) Spinocerebellar Ataxia Type 2
    English (Pseudonym) Spinocerebellar Ataxia Type 4
    English (Pseudonym) Spinocerebellar Ataxia Type 5
    English (Pseudonym) Spinocerebellar Ataxia Type 6
    English (Pseudonym) Spinocerebellar Ataxia Type 7
    English (Pseudonym) Spinocerebellar Atrophies
    Slovak (Pseudonym) ataxia spinocerebelárna, typ 1
    Slovak (Pseudonym) ataxia spinocerebelárna, typ 2
    Slovak (Pseudonym) ataxia spinocerebelárna, typ 4
    Slovak (Pseudonym) ataxia spinocerebelárna, typ 5
    Slovak (Pseudonym) ataxia spinocerebelárna, typ 6
    Slovak (Pseudonym) ataxia spinocerebelárna, typ 7
    Slovak (Pseudonym) atrofie spinocerebelárne
    See also(Skutočné meno) ataxíny
    (Skutočné meno) ataxín-1
    (Skutočné meno) ataxín-2
    (Skutočné meno) ataxín-3
    (Skutočné meno) ataxín-7
    (Later heading) ataxíny
    (Later heading) ataxín-1
    (Later heading) ataxín-2
    (Later heading) ataxín-3
    (Later heading) ataxín-7
    UDCC10.228.140.252.190.530C10.228.140.252.700.700C10.228.854.787.875C10.574.500.825.700C10.597.350.090.500.530C16.320.400.780.875
    NoteA group of 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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Number of the records: 1  

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