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Beta Thalassemia-HBB DeletionDuplication Analysis Test Cost

Original price was: 2,800 د.إ.Current price is: 2,100 د.إ.

-25%

The Beta Thalassemia-HBB Deletion/Duplication Analysis Test is a specialized genetic screening designed to identify deletions or duplications in the HBB gene, which are associated with beta thalassemia, a blood disorder that reduces the production of hemoglobin. Hemoglobin is essential for oxygen transport in the blood, and its deficiency leads to anemia and other related health issues. This test is crucial for individuals with a family history of beta thalassemia or those showing symptoms of the disorder, as it can provide definitive genetic evidence of the condition.

Performed at DNA Labs UAE, a leading facility in genetic diagnostics, the test ensures high accuracy and reliability. The process involves collecting a blood sample from the patient, which is then analyzed using advanced genetic testing techniques to detect any genetic abnormalities in the HBB gene.

The cost of the Beta Thalassemia-HBB Deletion/Duplication Analysis Test at DNA Labs UAE is 2100 AED. This investment in health can be invaluable for affected families, offering insights into genetic conditions, guiding treatment options, and helping in family planning decisions.

Description

Beta Thalassemia-HBB Deletion/Duplication Analysis Test

Test Name: Beta Thalassemia-HBB Deletion/Duplication Analysis Test

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

Price: 2100.0 AED

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

Report Delivery: 7-10 days

Method: MLPA (Multiplex Ligation-dependent Probe Amplification)

Test Type: Genetics

Doctor: Oncology

Test Department:

Pre Test Information: Beta Thalassemia-HBB deletion/duplication analysis 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 the beta-globin chains of hemoglobin. This can lead to anemia and other complications. HBB deletion/duplication analysis is a specific genetic test that looks for deletions or duplications in the HBB gene, which is responsible for encoding the beta-globin chains.

These types of mutations can disrupt the normal production of beta-globin chains and cause beta thalassemia. The analysis involves examining the DNA of an individual to determine if there are any deletions or duplications in the HBB gene. This can be done through various techniques, such as polymerase chain reaction (PCR) or fluorescence in situ hybridization (FISH).

The results of the analysis can help diagnose beta thalassemia and determine the specific type and severity of the condition. This information is important for guiding treatment decisions and providing appropriate genetic counseling.

Test Name	Beta Thalassemia-HBB deletionduplication analysis Test
Components	Sterile container / Sterile Normal Saline Container / EDTA Vacutainer (2ml)
Price	2100.0 AED
Sample Condition	Amniotic fluid \/ Chorionic villi \/ Cord blood\/Peripheral blood
Report Delivery	7-10 days
Method	MLPA
Test type	Genetics
Doctor	Oncology
Test Department:
Pre Test Information	Beta Thalassemia-HBB deletion/duplication 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. HBB deletion/duplication analysis is a specific genetic test that looks for deletions or duplications in the HBB gene, which is responsible for encoding the beta-globin chains. These types of mutations can disrupt the normal production of beta-globin chains and cause beta thalassemia. The analysis involves examining the DNA of an individual to determine if there are any deletions or duplications in the HBB gene. This can be done through various techniques, such as polymerase chain reaction (PCR) or fluorescence in situ hybridization (FISH). The results of the analysis can help diagnose beta thalassemia and determine the specific type and severity of the condition. This information is important for guiding treatment decisions and providing appropriate genetic counseling.