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HP Gene Anhaptoglobinemia Genetic Test Cost

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

-21%

The HP Gene Anhaptoglobinemia Genetic Test, available at DNA Labs UAE for a cost of 4400 AED, is a specialized diagnostic procedure aimed at identifying anhaptoglobinemia, a rare genetic condition characterized by the absence of haptoglobin in the blood. Haptoglobin is a protein responsible for binding free hemoglobin released from red blood cells, thus preventing it from causing harm to the body. Anhaptoglobinemia can lead to various health issues, including an increased risk of hemolytic anemia and cardiovascular disease.

This test specifically looks for mutations in the HP gene, which is responsible for the production of haptoglobin. By analyzing a sample of the patient’s DNA, the test can confirm the presence of these genetic alterations, providing crucial information for diagnosis and potential management of the condition. Conducted at the state-of-the-art facilities of DNA Labs UAE, the test adheres to high standards of accuracy and reliability, offering individuals a comprehensive understanding of their genetic health in relation to anhaptoglobinemia.

Description

HP Gene Anhaptoglobinemia Genetic Test

Test Name: HP Gene Anhaptoglobinemia Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

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 HP Gene Anhaptoglobinemia NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with HP Gene Anhaptoglobinemia NGS Genetic DNA Test gene HP

Test Details: HP Gene Anhaptoglobinemia NGS Genetic Test is a genetic test that uses next-generation sequencing (NGS) technology to analyze the HP gene for the presence of a specific genetic variant associated with anhaptoglobinemia. Anhaptoglobinemia is a rare genetic condition characterized by the absence or low levels of haptoglobin, a protein involved in binding and clearing free hemoglobin in the blood.

The test involves obtaining a DNA sample, usually through a blood sample or saliva swab, from the individual being tested. The DNA is then sequenced using NGS technology to identify any variations or mutations in the HP gene. The results of the test can determine if the individual has anhaptoglobinemia or carries a genetic variant associated with the condition.

This genetic test can be useful in diagnosing anhaptoglobinemia, especially in cases where clinical symptoms may not be apparent or when there is a family history of the condition. It can also help with genetic counseling and family planning decisions for individuals who are carriers of the genetic variant.

It is important to note that this test specifically targets the HP gene and is not a comprehensive genetic test for all possible genetic causes of anhaptoglobinemia. Other genetic tests may be necessary to rule out other potential causes of the condition. Additionally, the test may have limitations, such as the inability to detect certain rare or novel genetic variants.

Overall, the HP Gene Anhaptoglobinemia NGS Genetic Test is a specialized genetic test that can aid in the diagnosis and management of anhaptoglobinemia. It is typically performed by specialized laboratories or genetic testing companies and should be interpreted by a healthcare professional familiar with genetic testing and rare genetic conditions.

Test Name	HP Gene Anhaptoglobinemia 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 HP Gene Anhaptoglobinemia NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with HP Gene Anhaptoglobinemia NGS Genetic DNA Test gene HP
Test Details	HP Gene Anhaptoglobinemia NGS Genetic Test is a genetic test that uses next-generation sequencing (NGS) technology to analyze the HP gene for the presence of a specific genetic variant associated with anhaptoglobinemia. Anhaptoglobinemia is a rare genetic condition characterized by the absence or low levels of haptoglobin, a protein involved in binding and clearing free hemoglobin in the blood. The test involves obtaining a DNA sample, usually through a blood sample or saliva swab, from the individual being tested. The DNA is then sequenced using NGS technology to identify any variations or mutations in the HP gene. The results of the test can determine if the individual has anhaptoglobinemia or carries a genetic variant associated with the condition. This genetic test can be useful in diagnosing anhaptoglobinemia, especially in cases where clinical symptoms may not be apparent or when there is a family history of the condition. It can also help with genetic counseling and family planning decisions for individuals who are carriers of the genetic variant. It is important to note that this test specifically targets the HP gene and is not a comprehensive genetic test for all possible genetic causes of anhaptoglobinemia. Other genetic tests may be necessary to rule out other potential causes of the condition. Additionally, the test may have limitations, such as the inability to detect certain rare or novel genetic variants. Overall, the HP Gene Anhaptoglobinemia NGS Genetic Test is a specialized genetic test that can aid in the diagnosis and management of anhaptoglobinemia. It is typically performed by specialized laboratories or genetic testing companies and should be interpreted by a healthcare professional familiar with genetic testing and rare genetic conditions.