Sickle Cell Anemia Mutation Prenatal Diagnosis in Thalassery
Also known as: Sickle Cell Anemia Mutation Panel, Amniotic Fluid
Overview
A sickle variant in the DNA of a foetus causes red blood cells to take a sickle shape and can lead to various health problems. Sickle Cell Anemia Mutation Prenatal Diagnosis is a specialized genetic test performed during pregnancy to determine if the fetus carries the sickle cell variant. Sickle cell anemia is an inherited blood disorder caused by a specific mutation in the beta-globin gene (HBB) that leads to the production of abnormal hemoglobin S. This test is typically offered to couples who are known carriers of the sickle cell gene or have a family history of sickle cell anemia. The procedure involves analyzing a sample of fetal cells obtained through techniques such as chorionic villus sampling (CVS) or amniocentesis. By detecting the sickle variant in the fetus, prenatal diagnosis allows for early identification of sickle cell anemia, enabling parents to make informed decisions about their pregnancy and plan appropriate medical interventions or treatments for the affected child.
Sickle Cell Anemia Mutation Panel, Amniotic Fluid Price in Thalassery
Metropolis Healthcare is a leading diagnostics centre and pathology lab in India equipped with the latest state-of-the-art technologies that provides the Sickle Cell Anemia Mutation Panel, Amniotic Fluid with a clear pricing structure
The price of Sickle Cell Anemia Mutation Panel, Amniotic Fluid in Thalassery is ₹ 6,800
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Metropolis has a team of 200 senior pathologists and over 2000 technicians delivering diagnostic solutions in the areas of routine, semi specialty and super specialty domains like Oncology, Neurology, Gynaecology, Nephrology and many more.
We offer a comprehensive range of 4000+ clinical laboratory tests and profiles, which are used for prediction, early detection, diagnostic screening, confirmation and/or monitoring of the disease.
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