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  2. Non Invasive Prenatal Testing (NIPT) of trisomies 13, 18 et 21 and sex chromosomes

Non Invasive Prenatal Testing (NIPT) of trisomies 13, 18 et 21 and sex chromosomes

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Full name:
Non Invasive Prenatal Testing (NIPT) of trisomies 13, 18 et 21 and sex chromosomes
Test type:
Clinical
Test specialty:
Cytogenetics
Test purpose:
Prenatal diagnosis
Specimen:
Peripheral (whole) blood on EDTA
Method category:
Detection of chromosome alteration large in size
Method technique:
Next Generation Sequencing (NGS)
Laboratory:
Centrum Medische Genetica - UZ Brussel VUB
RIZIV code:
565611-565622
EQA:
  • 2015 NIPT for common aneuploidies Ringtest
  • 2016 NIPT for common aneuploidies Ringtest
  • 2017 NIPT for common aneuploidies GenQA (Genomics Quality Assessment)
  • 2018 NIPT for common aneuploidies GenQA (Genomics Quality Assessment)
  • 2019 NIPT for common aneuploidies GenQA (Genomics Quality Assessment)
  • 2020 NIPT for common aneuploidies GenQA (Genomics Quality Assessment)
  • 2021 NIPT for common aneuploidies GenQA (Genomics Quality Assessment)
  • 2022 NIPT for common aneuploidies GenQA (Genomics Quality Assessment)
Accreditation (ISO 15189):
2020-12-11 / 2021-06-14
Turnaround time (maximum):
5 working days
Document(s):
Created:
14 Dec 2019 - 10:59
Changed:
09 Mar 2023 - 16:20
URL:
https://laboguide.uzbrussel.be/laboguide#Analyses:NIPT&&&&&2516&&0