Beta Thalassemia-HBB Full Gene Analysis Couple and Prenatal Trio Analysis Test sale cost 3600 AED
NPM1 and FLT3 and CEBPA Test sale cost 3900 AED NPM1 and FLT3 and CEBPA Test Cost 5,200 د.إ Original price was: 5,200 د.إ.3,900 د.إCurrent price is: 3,900 د.إ.
Thalassemia Beta Trio Prenatal Mutation Detection Test sale cost 4210 AED Thalassemia Beta Trio Prenatal Mutation Detection Test Cost 4,680 د.إ Original price was: 4,680 د.إ.4,210 د.إCurrent price is: 4,210 د.إ.
Sale!

Beta Thalassemia-HBB Full Gene Analysis Couple and Prenatal Trio Analysis Test Cost

Original price was: 4,800 د.إ.Current price is: 3,600 د.إ.

-25%

Beta Thalassemia is a genetic blood disorder characterized by the reduction in the production of hemoglobin, which can lead to a range of health issues, including anemia, fatigue, and more severe complications if left untreated. The disorder is inherited, making genetic testing crucial for couples who have a family history of thalassemia or are carriers of the gene mutation.

The “Beta Thalassemia-HBB Full Gene Analysis Couple and Prenatal Trio Analysis Test” is a comprehensive genetic screening offered by DNA Labs UAE, designed to assess the risk of a couple passing on beta thalassemia to their offspring. This test specifically analyzes the HBB gene, which is implicated in beta thalassemia, to identify any mutations that may be present.

For couples considering starting a family, this test provides invaluable insights into their genetic makeup and the potential risk of their children inheriting beta thalassemia. It involves collecting DNA samples from both partners, which are then analyzed in the laboratory for any mutations in the HBB gene.

In addition to the couple’s analysis, the test also includes a prenatal trio analysis option, which can be performed during pregnancy to assess the fetus’s risk of inheriting the condition. This is particularly important for couples identified as carriers of the beta thalassemia gene mutation, as it allows for early intervention and planning.

The cost of the “Beta Thalassemia-HBB Full Gene Analysis Couple and Prenatal Trio Analysis Test” at DNA Labs UAE is 3600 AED. Given the comprehensive nature of this test and the detailed insights it provides into genetic risk factors for beta thalassemia, it represents a crucial step for at-risk couples in planning for a healthy family.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
Guaranteed Safe Checkout

Beta Thalassemia-HBB Full Gene Analysis Couple and Prenatal TRIO ANALYSIS Test

Test Name: Beta Thalassemia-HBB Full Gene Analysis Couple and Prenatal TRIO ANALYSIS Test

Components: Sterile container / Sterile Normal Saline Container / EDTA Vacutainer (2ml)

Price: 3600.0 AED

Sample Condition: Amniotic fluid / Chorionic villi / Cord blood / peripheral blood

Report Delivery: 8-10 days

Method: Sanger Sequencing

Test type: Genetics

Doctor: Gynecologist

Test Department:

Pre Test Information: Beta Thalassemia-HBB Full Gene Analysis (Couple + Prenatal) TRIO ANALYSIS] can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.

Test Details

Beta thalassemia is a genetic disorder characterized by reduced or absent production of the beta globin chains of hemoglobin. This can lead to anemia and other complications. A full gene analysis of the HBB gene is performed to identify any mutations or variants that may be associated with beta thalassemia.

This analysis is usually done on a couple who are planning to have a child, as well as on the fetus during prenatal testing. During a trio analysis, the genetic material of both parents and the fetus is analyzed to identify any genetic mutations or variants that may be present. This allows for a comprehensive assessment of the risk of beta thalassemia in the fetus.

The analysis involves sequencing the HBB gene to identify any mutations or variants that may be present. This can be done using various techniques, such as Sanger sequencing or next-generation sequencing. If any mutations or variants are identified, their pathogenicity and clinical significance are assessed. This information can help in determining the risk of beta thalassemia in the fetus and guide appropriate management and counseling.

Overall, a beta thalassemia-HBB full gene analysis (couple + prenatal) or trio analysis is an important tool in identifying the risk of beta thalassemia in couples planning to have a child and in providing accurate prenatal diagnosis and counseling.

Test Name Beta Thalassemia-HBB Full Gene Analysis Couple and Prenatal TRIO ANALYSIS Test
Components Sterile container / Sterile Normal Saline Container / EDTA Vacutainer (2ml)
Price 3600.0 AED
Sample Condition Amniotic fluid \/ Chorionic villi \/ Cord blood\/peripheral blood
Report Delivery 8-10 days
Method Sanger Sequencing
Test type Genetics
Doctor Gynecologist
Test Department:
Pre Test Information Beta Thalassemia-HBB Full Gene Analysis (Couple + Prenatal) TRIO ANALYSIS] can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad.
Test Details

Beta thalassemia is a genetic disorder characterized by reduced or absent production of the beta globin chains of hemoglobin. This can lead to anemia and other complications.

A full gene analysis of the HBB gene is performed to identify any mutations or variants that may be associated with beta thalassemia. This analysis is usually done on a couple who are planning to have a child, as well as on the fetus during prenatal testing.

During a trio analysis, the genetic material of both parents and the fetus is analyzed to identify any genetic mutations or variants that may be present. This allows for a comprehensive assessment of the risk of beta thalassemia in the fetus.

The analysis involves sequencing the HBB gene to identify any mutations or variants that may be present. This can be done using various techniques, such as Sanger sequencing or next-generation sequencing.

If any mutations or variants are identified, their pathogenicity and clinical significance are assessed. This information can help in determining the risk of beta thalassemia in the fetus and guide appropriate management and counseling.

Overall, a beta thalassemia-HBB full gene analysis (couple + prenatal) or trio analysis is an important tool in identifying the risk of beta thalassemia in couples planning to have a child and in providing accurate prenatal diagnosis and counseling.

SKU: TEST-4645 Category:

Related products