ALL MULTIPLEX PANEL (t(9;22),t(12;21),t(1;19),t(4;11)
- Report in 1 hr
- Serum
₹6,000
Price
₹10,000
or call 77900 98009
Alpha Thalassemia deletion/ duplication analysis by MLPA
₹10,000
Alpha thalassemia MLPA detects deletions and duplications in the HBA1 and HBA2 genes and their regulatory region, including common and rare deletions that routine tests may miss.
Results indicate the number of affected genes:
It also detects alpha gene duplications, which can worsen beta thalassemia. It guides carrier screening, couple counseling, and prenatal diagnosis. Point mutations need sequencing.
You should get an alpha thalassemia MLPA test if you have low MCV or MCH (small red cells) with normal iron levels and normal HbA2, or suspected HbH disease. It is also recommended for couples planning pregnancy with a family history of thalassemia, when both partners are carriers, for prenatal diagnosis, and for unexplained hydrops in pregnancy.
No special preparation or fasting is required for an alpha thalassemia MLPA test, as it analyzes DNA from a blood sample. Inform your doctor about any recent blood transfusion. Bring your previous CBC, Hb electrophoresis/HPLC, and iron study reports, along with your partner’s reports if available. Genetic counseling is recommended before and after testing.
No, fasting is not required for an alpha thalassemia MLPA test. You can eat and drink normally before giving your sample, because the test analyzes your DNA, which is not affected by food or the time of day. Inform your doctor about any recent blood transfusion.
₹6,000
₹8,000
₹15,000
₹7,000
Tell us what your doctor has prescribed and our team will confirm the right test and book it for you.