Beta-globin hemoglobinopathies, Sickle cell anemia, Sickle cell disorder (hot spot mutation - p.Glu6Val, p.Glu6Lys)

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Full name:
Beta-globin hemoglobinopathies, Sickle cell anemia, Sickle cell disorder (hot spot mutation - p.Glu6Val, p.Glu6Lys)
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Carrier diagnosis,
Post-natal Diagnosis,
Prenatal diagnosis
Specimen:
Peripheral (whole) blood on EDTA,
Amniotic fluid,
Chorionic villi
Method category:
Method technique:
Laboratory:
RIZIV code:
EQA:
  • 2015 DNA for Haemoglobinopathies UK NEQAS Haematology and Transfusion
  • 2016 DNA for Haemoglobinopathies UK NEQAS Haematology and Transfusion
  • 2017 DNA for Haemoglobinopathies UK NEQAS Haematology and Transfusion
  • 2018 DNA for Haemoglobinopathies UK NEQAS Haematology and Transfusion
  • 2019 DNA for Haemoglobinopathies UK NEQAS Haematology and Transfusion
  • 2020 DNA for Haemoglobinopathies UK NEQAS Haematology and Transfusion
  • 2021 DNA for Haemoglobinopathies UK NEQAS Haematology and Transfusion
  • 2022 DNA for Haemoglobinopathies UK NEQAS Haematology and Transfusion
  • 2023 DNA for Haemoglobinopathies UK NEQAS Haematology and Transfusion
Accreditation (ISO 15189):
2021-03-25 / 2024-09-10
Turnaround time (maximum):
2 months
Document(s):
Created:
22 Aug 2019 - 10:02
Changed:
19 Jan 2024 - 09:02
URL: