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  2. Hirschsprung disease

Hirschsprung disease

Genetic test Export to PDF
Full name:
Hirschsprung disease
Description:

Part of the Onco-endocrine pathologies panel (Panel OE)
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:
Sequence analysis: entire coding region
Deletion/duplication analysis
Method technique:
Next Generation Sequencing (NGS)
Laboratory:
Centre de Génétique Médicale UCL
RIZIV code:
565471-565482
Turnaround time (maximum):
3 months
Document(s):
Created:
16 Jan 2020 - 13:36
Changed:
11 Dec 2023 - 12:11