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Fragile X syndrome/POF/FXTAS - CGG repeat expansion

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Full name:
Fragile X syndrome/POF/FXTAS - CGG repeat expansion
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Carrier diagnosis,
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
Southern blot
Laboratory:
Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
RIZIV code:
565375-565386
EQA:
  • 2015 Fragile X Syndrome EMQN
  • 2018 Fragile X Syndrome EMQN
  • 2021 Fragile X Syndrome EMQN
  • 2022 Fragile X Syndrome EMQN
Accreditation (ISO 15189):
2022-10-07 / 2027-10-06
Turnaround time (maximum):
10 - 15 days
Created:
19 Jul 2019 - 10:55
Changed:
04 Dec 2023 - 10:04