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HBG2 Gene Hereditary Persistence of Fetal Hemoglobin Genetic Test

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The HBG2 gene hereditary persistence of fetal hemoglobin (HPFH) genetic test is a specialized diagnostic procedure aimed at detecting mutations in the HBG2 gene. These mutations are associated with the hereditary persistence of fetal hemoglobin (HPFH), a condition where individuals continue to produce fetal hemoglobin (HbF) at elevated levels into adulthood. Normally, the production of HbF, which has a high affinity for oxygen, ceases after birth, and its expression is replaced by adult hemoglobin. However, in HPFH, the elevated levels of HbF can ameliorate symptoms of hemoglobinopathies like beta-thalassemia and sickle cell disease, leading to a milder clinical presentation.

The test involves analyzing the patient’s DNA, extracted from a blood sample, to identify specific genetic variations or mutations in the HBG2 gene that are known to cause HPFH. This genetic testing is crucial for individuals with a family history of HPFH or related hemoglobin disorders, as it can provide valuable information for disease management and genetic counseling.

Performed at DNA Labs UAE, a leading provider of genetic testing services in the region, the HBG2 gene HPFH genetic test is priced at 4400 AED. DNA Labs UAE is equipped with state-of-the-art technology and staffed by experienced geneticists and laboratory technicians, ensuring high-quality and accurate testing results. This test is an essential tool for the early diagnosis and management of HPFH, helping affected individuals and their families make informed health and lifestyle decisions.

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HBG2 Gene Hereditary Persistence of Fetal Hemoglobin Genetic Test

Components

  • Price: 4400.0 AED
  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
  • Report Delivery: 3 to 4 Weeks
  • Method: NGS Technology
  • Test type: Hematology
  • Doctor: Hematologist
  • Test Department: Genetics

Pre Test Information

Clinical History of Patient who is going for HBG2 Gene Hereditary persistence of fetal hemoglobin NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with HBG2 Gene Hereditary persistence of fetal hemoglobin NGS Genetic DNA Test gene HBG2.

Test Details

The HBG2 gene is responsible for producing the fetal hemoglobin protein. Hereditary persistence of fetal hemoglobin (HPFH) is a condition where individuals continue to produce fetal hemoglobin into adulthood instead of transitioning to adult hemoglobin. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual. In the context of HBG2 gene and HPFH, NGS genetic testing can be used to identify any mutations or variations in the HBG2 gene that may be responsible for the condition. By sequencing the entire HBG2 gene, NGS testing can provide detailed information about any genetic changes that may be present. This can help in the diagnosis of HPFH and provide insights into the inheritance pattern of the condition within a family.

NGS genetic testing is a powerful tool that allows for the analysis of multiple genes simultaneously and can provide a comprehensive view of an individual’s genetic makeup. It can be used to identify mutations, determine carrier status, and provide information about the risk of developing certain genetic conditions. In the case of HBG2 gene and HPFH, NGS genetic testing can be particularly useful in diagnosing the condition and providing information about the risk of passing it on to future generations. It can also be used to guide treatment decisions and provide genetic counseling to affected individuals and their families.

Test Name HBG2 Gene Hereditary persistence of fetal hemoglobin Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Hematology
Doctor Hematologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for HBG2 Gene Hereditary persistence of fetal hemoglobin NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with HBG2 Gene Hereditary persistence of fetal hemoglobin NGS Genetic DNA Test gene HBG2
Test Details

The HBG2 gene is responsible for producing the fetal hemoglobin protein. Hereditary persistence of fetal hemoglobin (HPFH) is a condition where individuals continue to produce fetal hemoglobin into adulthood instead of transitioning to adult hemoglobin.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual. In the context of HBG2 gene and HPFH, NGS genetic testing can be used to identify any mutations or variations in the HBG2 gene that may be responsible for the condition.

By sequencing the entire HBG2 gene, NGS testing can provide detailed information about any genetic changes that may be present. This can help in the diagnosis of HPFH and provide insights into the inheritance pattern of the condition within a family.

NGS genetic testing is a powerful tool that allows for the analysis of multiple genes simultaneously and can provide a comprehensive view of an individual’s genetic makeup. It can be used to identify mutations, determine carrier status, and provide information about the risk of developing certain genetic conditions.

In the case of HBG2 gene and HPFH, NGS genetic testing can be particularly useful in diagnosing the condition and providing information about the risk of passing it on to future generations. It can also be used to guide treatment decisions and provide genetic counseling to affected individuals and their families.

SKU: TEST-3913 Category:

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