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CR1 Gene CR1 deficiency Genetic Test

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

-21%

The CR1 gene, also known as Complement Receptor 1, plays a crucial role in the immune system by mediating the clearance of immune complexes and modulating complement activation. CR1 deficiency is a rare genetic condition that can lead to an increased susceptibility to infections, autoimmune disorders, and certain types of hemolytic anemia, due to the impaired ability of the immune system to clear complexes and properly regulate complement activation.

A genetic test for CR1 deficiency can provide valuable information for individuals who may be at risk of this condition, either due to familial history or symptoms suggestive of complement system disorders. This test involves analyzing the DNA to identify mutations in the CR1 gene that could lead to reduced function or expression of the CR1 protein.

In the United Arab Emirates, DNA Labs UAE offers a comprehensive genetic test for CR1 deficiency. The cost of the test is 4400 AED. This test is performed in a state-of-the-art laboratory facility, where experienced professionals use advanced genetic sequencing technologies to ensure accurate and reliable results. Upon completion of the test, individuals receive a detailed report that can be used to guide further medical consultation and potential treatment options. It is an essential tool for those seeking to understand their genetic predisposition to CR1-related conditions and to take proactive steps in managing their health.

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CR1 Gene CR1 deficiency Genetic Test

At DNA Labs UAE, we offer the CR1 Gene CR1 deficiency Genetic Test at a cost of AED 4400.0.

Test Details

The CR1 gene encodes for the complement receptor type 1 protein, which is involved in the regulation of the immune system. CR1 deficiency refers to a condition where there is a reduced or absent expression of the CR1 protein.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. In the context of CR1 deficiency, NGS genetic testing can be used to identify mutations or variations in the CR1 gene that may be responsible for the deficiency. By analyzing the entire coding region of the CR1 gene, NGS can provide a comprehensive assessment of genetic variants that may be associated with CR1 deficiency.

This can help in diagnosing the condition, understanding its inheritance pattern, and providing appropriate genetic counseling and management strategies. NGS genetic testing can also be used to identify other genetic variants or mutations in other genes that may be associated with similar clinical features or conditions, thus providing a more comprehensive evaluation of the individual’s genetic profile.

It is important to note that NGS genetic testing should be performed and interpreted by trained healthcare professionals who specialize in genetics, as the results may have implications for the individual’s health and the health of their family members. Genetic counseling is typically recommended before and after genetic testing to ensure a thorough understanding of the testing process and its implications.

Test Name: CR1 Gene CR1 deficiency 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: Cardiovascular Pneumology Disorders

Doctor: Cardiologist

Test Department: Genetics

Pre Test Information

Clinical History of Patient who is going for CR1 Gene CR1 deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CR1 Gene CR1 deficiency NGS Genetic DNA Test gene CR1.

Test Name CR1 Gene CR1 deficiency 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 Cardiovascular Pneumology Disorders
Doctor Cardiologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for CR1 Gene CR1 deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CR1 Gene CR1 deficiency NGS Genetic DNA Test gene CR1
Test Details

The CR1 gene encodes for the complement receptor type 1 protein, which is involved in the regulation of the immune system. CR1 deficiency refers to a condition where there is a reduced or absent expression of the CR1 protein.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. In the context of CR1 deficiency, NGS genetic testing can be used to identify mutations or variations in the CR1 gene that may be responsible for the deficiency.

By analyzing the entire coding region of the CR1 gene, NGS can provide a comprehensive assessment of genetic variants that may be associated with CR1 deficiency. This can help in diagnosing the condition, understanding its inheritance pattern, and providing appropriate genetic counseling and management strategies.

NGS genetic testing can also be used to identify other genetic variants or mutations in other genes that may be associated with similar clinical features or conditions, thus providing a more comprehensive evaluation of the individual’s genetic profile.

It is important to note that NGS genetic testing should be performed and interpreted by trained healthcare professionals who specialize in genetics, as the results may have implications for the individual’s health and the health of their family members. Genetic counseling is typically recommended before and after genetic testing to ensure a thorough understanding of the testing process and its implications.