1. Genetic tests
  2. Spinocerebellar ataxia (types 1, 2, 3, 6, 7) - CAG repeat expansion

Spinocerebellar ataxia (types 1, 2, 3, 6, 7) - CAG repeat expansion

Genetic test Export to PDF
Full name:
Spinocerebellar ataxia (types 1, 2, 3, 6, 7) - CAG repeat expansion
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Carrier diagnosis,
Mutation confirmation,
Post-natal Diagnosis,
Pre-implantation genetic diagnosis,
Predictive and Pre-symptomatic diagnosis,
Prenatal diagnosis
Specimen:
Peripheral (whole) blood on EDTA,
Amniotic fluid,
Chorionic villi,
Cell culture
Method category:
Targeted variant analysis
Method technique:
PCR based technique
Laboratory:
Centrum Medische Genetica - UZ Brussel VUB
RIZIV code:
565471-565482
EQA:
  • 2015 Spinocerebellar Ataxia’s EMQN
  • 2016 Spinocerebellar Ataxia’s EMQN
  • 2017 Spinocerebellar Ataxia’s EMQN
  • 2018 Spinocerebellar Ataxia’s EMQN
  • 2019 Spinocerebellar Ataxia’s EMQN
  • 2020 Spinocerebellar Ataxia’s EMQN
  • 2021 Spinocerebellar Ataxia’s EMQN
  • 2022 Spinocerebellar Ataxia’s EMQN
Turnaround time (maximum):
3 months (10 working days for prenatal diagnosis)
Document(s):
Created:
23 Jul 2019 - 12:23
Changed:
09 Mar 2023 - 16:30
URL:
https://laboguide.uzbrussel.be/laboguide#Analyses:Spinocerebellaire%20ataxie