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Alpha-Thalassemia (21 α-Globin Gene Mutations) by PCR

Accredited Facility E-report Qualified Specialists

This PCR-based genetic test detects common mutations in the alpha-globin genes associated with Alpha thalassemia. It helps diagnose alpha-thalassemia and identify carrier status.

  • If alpha-thalassemia is suspected.
  • During evaluation of unexplained anemia or microcytosis.
  • For carrier screening before marriage or pregnancy.
  • When there is family history of thalassemia.
  • As part of genetic or hematology assessment.
  • No fasting is usually required.
  • A blood sample will be collected from a vein.
  • Genetic counseling may be recommended in some cases.
  • Inform the healthcare provider about family history of blood disorders.
  • Follow all laboratory instructions before sample collection.
  • Alpha-Thalassemia (21 α-Globin Gene Mutations) by PCR
    No labs currently offering this test.