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Recessive nonsyndromic hearing loss and deafness (2 genes)

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Full name:
Recessive nonsyndromic hearing loss and deafness (2 genes)
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Carrier diagnosis,
Post-natal Diagnosis,
Prenatal diagnosis
Specimen:
Peripheral (whole) blood on EDTA,
Chorionic villi,
Amniotic fluid
Method category:
Targeted variant analysis
Sequence analysis: entire coding region
Method technique:
PCR based technique
Bi-directional Sanger Sequence analysis
Laboratory:
Centre de Génétique Humaine - CHU Sart-Tilman
RIZIV code:
565456-565460
EQA:
  • 2015 Hereditary deafness EMQN
  • 2019 Hereditary deafness EMQN
  • 2022 Hereditary deafness EMQN
Accreditation (ISO 15189):
2022-02-24 / 2026-02-23
Turnaround time (maximum):
2 weeks
Document(s):
Created:
29 Jul 2019 - 17:06
Changed:
23 Jan 2023 - 13:31
URL:
https://www.chu.ulg.ac.be/jcms/c_525432/fr/surdite-neurosensorielle-congenitale