Diagnosis:
Spinocerebellar ataxia, dominantly inherited forms (SCA, SCA1, SCA2, SCA6, SCA7, SCA8)
Information/Diagnosedescriptions
- Socialstyrelsen. Videnscenter for Handicap, Hjælpemidler og Socialpsykiatri (Danish)
- Maskun Neurologinen Kuntoutuskeskus (Suomi)
- Socialstyrelsens kunskapsdatabas om små och mindre kända handikappgrupper (Swedish)
- The National Board of Health and Welfare (Swedish)
Sorry, but there is no nordic information in english about this diagnosis. Please get in touch with one the nordic sentres
Get in touch
- Foreningen for Ataksi/HSP
- Ataksiaverkosto/Neuroliitto ry
- Norsk forening for Arvelig -Spastisk Paraparese/-Ataksi (NASPA)
Sorry, Rarelink do not inform about english contacts.
Other descriptions "Spinocerebellar ataxia, dominantly inherited forms"
English
- Machado-Joseph disease/Spinocerebellar ataxia 3
- SCA, SCA1, SCA2, SCA6, SCA7, SCA8
Suomi
- Spinoserebellaarinen ataksia tyyppi 3 (SCA3)
- Machado-Josephin tauti (MJD)
- SCA 3
- Spinoserebellaarinen atrofia III
Swedish
- Spinocerebellära ataxier, dominant ärftliga
- Machado-Josephs sjukdom/SCA3
- SCA
- SCA1
- SCA2
- SCA3/Machado-Josephs sjukdom
- SCA6
- SCA7
- SCA8
Norwegian
- Machado-Joseph sykdom
- Spinocerebellær ataksi 3
Danish
- Machado-Joseph
- SCA 3
Information
The information and descriptions of diagnoses is found through links to external pages (outside rarelink)A
diagnoses can be listed under several names, in both english and nordic languages.
