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Beta Thalassemia-HBB Full Gene Analysis Couple Test Cost

Original price was: 4,000 د.إ.Current price is: 3,000 د.إ.

-25%

The “Beta Thalassemia-HBB Full Gene Analysis Couple Test” offered by DNA Labs UAE is a comprehensive genetic screening designed for couples who want to assess their risk of passing beta thalassemia to their offspring. Beta thalassemia is a blood disorder that reduces the production of hemoglobin, leading to anemia and various health complications. This condition is inherited in an autosomal recessive pattern, meaning both parents must carry the mutated gene to pass the disorder to their children.

The test involves analyzing the HBB gene, which is responsible for the production of the beta-globin component of hemoglobin. Mutations in this gene are the primary cause of beta thalassemia. By examining the full gene, the test can identify specific mutations that both partners carry, providing a comprehensive risk assessment for their potential children.

Priced at 3000 AED, the test is conducted in the advanced facilities of DNA Labs UAE, ensuring accuracy and reliability. The test results can help couples make informed decisions about family planning, and when a risk is identified, they can explore options such as genetic counseling or in vitro fertilization (IVF) with preimplantation genetic diagnosis (PGD) to reduce the likelihood of having a child affected by beta thalassemia.

Overall, the “Beta Thalassemia-HBB Full Gene Analysis Couple Test” is a valuable resource for couples looking to understand their genetic risks and make informed decisions about their future family’s health.

Description

Beta Thalassemia-HBB Full Gene Analysis Couple Test

Test Name: Beta Thalassemia-HBB Full Gene Analysis Couple Test

Components: EDTA Vacutainer (2ml)

Price: 3000.0 AED

Sample Condition: 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) can be done with a Doctor’s 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 beta-globin chains, leading to a decrease in the production of hemoglobin. This disorder is caused by mutations in the HBB gene.

A full gene analysis of the HBB gene in a couple would involve sequencing the entire coding region and intron-exon boundaries of the gene. This analysis would identify any mutations or variations in the HBB gene that may be associated with beta thalassemia.

The analysis would typically involve obtaining a blood sample from each individual in the couple. The DNA would then be extracted from the blood cells and subjected to sequencing techniques to determine the nucleotide sequence of the HBB gene.

The results of the analysis would be compared to a reference sequence to identify any mutations or variations. If any disease-causing mutations are found in one or both individuals, they would be considered carriers of beta thalassemia. If both individuals are carriers, there is a risk of having a child with beta thalassemia.

Genetic counseling would be recommended to discuss the implications of the results and the options available for family planning, such as prenatal testing or assisted reproductive technologies.

Test Name	Beta Thalassemia-HBB Full Gene Analysis Couple Test
Components	EDTA Vacutainer (2ml)
Price	3000.0 AED
Sample Condition	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) 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 beta-globin chains, leading to a decrease in the production of hemoglobin. This disorder is caused by mutations in the HBB gene. A full gene analysis of the HBB gene in a couple would involve sequencing the entire coding region and intron-exon boundaries of the gene. This analysis would identify any mutations or variations in the HBB gene that may be associated with beta thalassemia. The analysis would typically involve obtaining a blood sample from each individual in the couple. The DNA would then be extracted from the blood cells and subjected to sequencing techniques to determine the nucleotide sequence of the HBB gene. The results of the analysis would be compared to a reference sequence to identify any mutations or variations. If any disease-causing mutations are found in one or both individuals, they would be considered carriers of beta thalassemia. If both individuals are carriers, there is a risk of having a child with beta thalassemia. Genetic counseling would be recommended to discuss the implications of the results and the options available for family planning, such as prenatal testing or assisted reproductive technologies.