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Steinert myotonic dystrophy - CTG repeat expansion

Genetic test Export to PDF
Full name:
Steinert myotonic dystrophy - CTG repeat expansion
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Post-natal Diagnosis,
Prenatal diagnosis
Specimen:
Peripheral (whole) blood on EDTA,
Amniotic fluid,
Chorionic villi
Method category:
Targeted variant analysis
Method technique:
PCR based technique
Laboratory:
Centre de Génétique Humaine - CHU Sart-Tilman
RIZIV code:
565456-565460
EQA:
  • 2015 Myotonic Dystrophy EMQN
  • 2020 Myotonic Dystrophy EMQN
  • 2022 Myotonic Dystrophy EMQN
Accreditation (ISO 15189):
2022-02-24 / 2026-02-23
Turnaround time (maximum):
2 mois
Document(s):
Created:
31 Jul 2019 - 13:59
Changed:
23 Jan 2023 - 13:37
URL:
https://www.chuliege.be/jcms/c_525336/fr/myopathie-de-steinert