1. Genetic tests
  2. Angelman / Prader Willi Syndrome

Angelman / Prader Willi Syndrome

Genetic test Export to PDF
Full name:
Angelman / Prader Willi Syndrome
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Post-natal Diagnosis,
Prenatal diagnosis
Specimen:
Peripheral (whole) blood on EDTA,
Amniotic fluid
Method category:
Methylation analysis
Deletion/duplication analysis
Method technique:
MLPA based techniques
Laboratory:
Centre de Génétique Médicale UCL
RIZIV code:
565456-565460
EQA:
  • 2015 Prader-Willi and Angelman Syndromes EMQN
  • 2016 Prader-Willi and Angelman Syndromes EMQN
  • 2017 Prader-Willi and Angelman Syndromes EMQN
  • 2018 Prader-Willi and Angelman Syndromes EMQN
  • 2020 Prader-Willi and Angelman Syndromes EMQN
  • 2022 Prader-Willi and Angelman Syndromes EMQN
Accreditation (ISO 15189):
2022-12-22 / 2027-12-21
Turnaround time (maximum):
3 months
Document(s):
Created:
24 Jul 2019 - 11:08
Changed:
24 Jan 2023 - 14:36