Frequent hearing deficiency (4 genes)

Genetic test Export to PDF
Full name:
Frequent hearing deficiency (4 genes)
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:
Method technique:
Laboratory:
RIZIV code:
EQA:
  • 2017 Hereditary deafness EMQN
  • 2018 Hereditary deafness EMQN
  • 2019 Hereditary deafness EMQN
  • 2020 Hereditary deafness EMQN
  • 2021 Hereditary deafness EMQN
  • 2022 Hereditary deafness EMQN
  • 2023 Hereditary deafness EMQN
Accreditation (ISO 15189):
2021-03-25 / 2024-09-09
Turnaround time (maximum):
3 months
Document(s):
Created:
29 Jul 2019 - 17:06
Changed:
19 Jan 2024 - 09:20
URL: