1. Genetic tests
  2. Pheochromocytoma - paraganglioma syndrome (gene panel)

Pheochromocytoma - paraganglioma syndrome (gene panel)

Genetic test Export to PDF
Full name:
Pheochromocytoma - paraganglioma syndrome (gene panel)
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Post-natal Diagnosis,
Predictive and Pre-symptomatic diagnosis
Specimen:
Peripheral (whole) blood on EDTA
Method category:
Sequence analysis: entire coding region
Deletion/duplication analysis
Method technique:
MLPA based techniques
Next Generation Sequencing (NGS)
Laboratory:
Centrum Medische Genetica - UZ Gent
RIZIV code:
565530-565541
EQA:
  • 2019 Phaeochromocytoma and Paraganglioma Disorders EMQN
Accreditation (ISO 15189):
2021-09-11 / 2026-09-10
Turnaround time (maximum):
3 - 4 months
Document(s):
Created:
22 Jul 2019 - 14:27
Changed:
13 Dec 2022 - 11:54
  • Pheochromocytoma - paraganglioma syndrome - UGent
    Gene % of coding sequence sufficiently covered to detect heterozygous mutations Copy number variation Comments
    MAX 100.00 1
    RET 100.00 0
    SDHA 100.00 1
    SDHAF2 100.00 1
    SDHB 100.00 1
    SDHC 100.00 1
    SDHD 100.00 1
    TMEM127 100.00 1
    VHL 100.00 1
    SUCLG2 100.00 0