Evidence for a common Spinocerebellar ataxia type 7 (SCA7) founder mutation in Scandinavia

Eur J Hum Genet. 2000 Dec;8(12):918-22. doi: 10.1038/sj.ejhg.5200557.


Spinocerebellar ataxia type 7 (SCA7) is a neuro-degenerative disorder characterised by progressive cerebellar ataxia and macular degeneration. SCA7 is one of the least common genetically verified autosomal dominant cerebellar ataxias (ADCAs) in the world (4.5 to 11.6%), but in Sweden and Finland SCA7 is the most commonly identified form of ADCA. In an inventory of hereditary ataxias in Scandinavia (Sweden, Norway, Denmark and Finland) we identified 15 SCA7 families, eight in Sweden and seven in Finland, while no cases of SCA7 could be found in Norway or Denmark. We examined whether the relatively high frequency of SCA7 families in Sweden and Finland was the result of a common founder effect. Only two out of 15 families could be connected genealogically. However, an extensive haplotype analysis over a 10.2 cM region surrounding the SCA7 gene locus showed that all 15 families studied shared a common haplotype over at least 1.9 cM. This strongly suggests that all Scandinavian SCA7 families originate from a common founder pre-mutation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ataxin-7
  • Female
  • Finland
  • Founder Effect*
  • Haplotypes
  • Humans
  • Male
  • Mutation
  • Nerve Tissue Proteins / genetics*
  • Spinocerebellar Ataxias / genetics*
  • Sweden


  • ATXN7 protein, human
  • Ataxin-7
  • Nerve Tissue Proteins