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,
Chorionic villi
Method category:
Methylation analysis
Deletion/duplication analysis
Method technique:
MLPA based techniques
Laboratory:
Centrum Medische Genetica - UZ Gent
RIZIV code:
565456-565460
EQA:
  • 2015 Prader-Willi and Angelman Syndromes EMQN
  • 2016 Prader-Willi and Angelman Syndromes EMQN
  • 2018 Prader-Willi and Angelman Syndromes EMQN
  • 2020 Prader-Willi and Angelman Syndromes EMQN
Accreditation (ISO 15189):
2021-09-11 / 2026-09-10
Turnaround time (maximum):
6 weeks
Document(s):
Created:
17 Jul 2019 - 13:32
Changed:
13 May 2022 - 12:20