SCA17

Abbreviation for:
spinocerebellar ataxia type 17 (see there)

References in periodicals archive ?

[sup][5],[6] SCA1, SCA2, SCA3/MJD, SCA6, SCA7, SCA12, SCA17 and dentatorubral-pallidoluysian atrophy (DRPLA) share the most prevalent form of unstable CAG repeats.

The repeat-containing regions of the genes causing SCA1, SCA2, SCA3/MJD, SCA6, SCA7, SCA8, SCA12, SCA17 and DRPLA were amplified using appropriate primer pairs with polymerase chain reaction (PCR) [Table 1].

In our study, the genetic testing of Family J, which presented clinically diagnosed SCA, was not in agreement with the known subtypes of SCA1, SCA2, SCA3/MJD, SCA6, SCA7, SCA8, SCA12, SCA17 and DRPLA.

Clinical Characteristics, Radiological Features and Gene Mutation in 10 Chinese Families with Spinocerebellar Ataxias

and 1.6% for SCA17. They identified six individuals with the rare allele

Enfermedades neurodegenerativas: la ataxia espinocerebelosa tipo 7 en Mexico

SCA17 repeat sizes were determined using previously described methods.

A single individual was diagnosed with SCA17. Molecular diagnostic testing for SCA17 was introduced in 2005, and is therefore excluded from the analysis of the full 24-year period.