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Hypercholesterolemia, Familial (gene panel)

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Full name:
Hypercholesterolemia, Familial (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:
Next Generation Sequencing (NGS)
MLPA based techniques
Laboratory:
Centrum Medische Genetica - UZ Antwerpen
RIZIV code:
565471-565482
EQA:
  • 2019 Familial autosomal dominant hypercholesterolemia EMQN
  • 2022 Familial autosomal dominant hypercholesterolemia EMQN
Accreditation (ISO 15189):
2023-11-09 / 2024-05-08
Turnaround time (maximum):
4 months
Document(s):
Created:
19 Jul 2019 - 13:01
Changed:
22 Jan 2024 - 13:50
URL:
https://labogidsmedgen.uza.be/analyses/familiale-hypercholesterolemie-chol