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Recessive nonsyndromic hearing loss and deafness DFNB (2 genes)

Genetic test Export to PDF
Full name:
Recessive nonsyndromic hearing loss and deafness DFNB (2 genes)
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Carrier diagnosis,
Post-natal Diagnosis
Specimen:
Peripheral (whole) blood on EDTA,
Amniotic fluid,
Chorionic villi
Method category:
Targeted variant analysis
Sequence analysis: entire coding region
Method technique:
PCR based technique
Bi-directional Sanger Sequence analysis
Laboratory:
Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
RIZIV code:
565456-565460
EQA:
  • 2015 Hereditary deafness EMQN
  • 2018 Hereditary deafness EMQN
  • 2021 Hereditary deafness EMQN
Turnaround time (maximum):
20 - 60 days
Document(s):
Created:
29 Jul 2019 - 17:06
Changed:
26 Apr 2022 - 15:02