1. Genetic tests
  2. Phenylketonuria

Phenylketonuria

Genetic test Export to PDF
Full name:
Phenylketonuria
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:
Sequence analysis: entire coding region
Deletion/duplication analysis
Method technique:
Next Generation Sequencing (NGS)
MLPA based techniques
Laboratory:
Centre de Génétique Humaine - Erasme ULB
RIZIV code:
565471-565482
EQA:
  • 2019 Phenylketonuria EMQN
  • 2022 Phenylketonuria EMQN
Accreditation (ISO 15189):
2021-03-25 / 2024-09-09
Turnaround time (maximum):
3 months
Document(s):
Created:
23 Aug 2019 - 07:20
Changed:
18 Aug 2023 - 09:31
URL:
https://ulbgenetics.be/compendium-des-analyses/#GM65