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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:
Centrum Medische Genetica - UZ Gent
RIZIV code:
565456-565460
EQA:
  • 2015 Myotonic Dystrophy EMQN
  • 2017 Myotonic Dystrophy EMQN
  • 2019 Myotonic Dystrophy EMQN
  • 2020 Myotonic Dystrophy EMQN
Accreditation (ISO 15189):
2021-09-11 / 2026-09-10
Turnaround time (maximum):
6 weeks
Document(s):
Created:
31 Jul 2019 - 13:59
Changed:
20 May 2022 - 11:05