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This test is used to diagnose mutations in the HBB gene in sickle cell anemia. This determines the maternal cell taint in amniotic fluid. This test is done during pregnancy as the mutation in the fetus is to be examined. This enables the early detection of any mutation-related disease during pregnancy only.
It is a yellow and clear fluid that surrounds the baby in the womb of the Mother during pregnancy. The amniotic sac is covered around it. The womb is buoyant in the amniotic sac. It plays the following functions:
In specific conditions, the DNA sequence may experience a difference that can be fatal; this is known as Mutation. This usually originates due to environmental justifications also. It is of the following two types-
There is a tinier carriage of oxygen in our bodies. Anemia is mainly caused due to a reduction in levels of iron. Anemia may be -
Mutations in HBB genes cause sickle cell anemia. The cells become the same as the shape of a disc. The lifespan of sickle cells is less and disturbs the body's function. The oxygen-carrying capacity of RBCs RBC's altered.
The following medicines are prescribed: Hydroxyurea (Hydrea)
| Test Type | Sickle Cell Anemia Trio Prenatal Mutation Detection |
| Includes | Sickle Cell Anemia Trio Prenatal Mutation Detection Test (Pathology Test) |
| Preparation | |
| Reporting | Within 24 hours* |
| Test Price |
₹ 9750
|
Early check ups are always better than delayed ones. Safety, precaution & care is depicted from the several health checkups. Here, we present simple & comprehensive health packages for any kind of testing to ensure the early prescribed treatment to safeguard your health.
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