CR1 Gene CR1 deficiency Genetic Test
At DNA Labs UAE, we offer the CR1 Gene CR1 deficiency Genetic Test for individuals who suspect they may have CR1 deficiency. This test helps identify mutations or variants in the CR1 gene, which is responsible for encoding the complement receptor 1 (CR1) protein. CR1 deficiency is a rare genetic disorder that can lead to an overactive complement system and cause inflammation and tissue damage.
Test Components and Price
The CR1 Gene CR1 deficiency Genetic Test is priced at 4400.0 AED. The test requires a blood sample or extracted DNA, or one drop of blood on an FTA card. Our laboratory uses NGS (Next-Generation Sequencing) technology to analyze multiple genes simultaneously, providing a comprehensive view of an individual’s genetic makeup.
Report Delivery and Test Department
After the sample is collected, the report will be delivered within 3 to 4 weeks. Our test department specializes in genetics and is staffed by experienced professionals who ensure accurate and timely results.
Test Type and Doctor
The CR1 Gene CR1 deficiency Genetic Test falls under the category of neurological disorders. It is recommended to consult with a neurologist who can provide further guidance and interpretation of the test results.
Pre Test Information
Prior to undergoing the CR1 Gene CR1 deficiency Genetic Test, it is essential to provide the clinical history of the patient. Additionally, a genetic counseling session is recommended to draw a pedigree chart of family members affected by CR1 Gene CR1 deficiency. This information helps in understanding the inheritance pattern and assessing the risk of developing the disorder.
Understanding CR1 Gene CR1 deficiency
The CR1 gene encodes the complement receptor 1 (CR1) protein, which plays a crucial role in regulating the complement system. CR1 deficiency is a rare genetic disorder characterized by a decrease or absence of CR1 protein on the surface of red blood cells and other cells in the body. This can result in an overactive complement system, leading to inflammation and tissue damage.
When to Consider the Test
Genetic testing for CR1 deficiency may be recommended for individuals with a family history of the disorder or those experiencing symptoms such as recurrent infections, hemolytic anemia, or kidney disease. Early diagnosis and management of CR1 deficiency can help prevent complications and improve outcomes.
At DNA Labs UAE, we understand the importance of accurate and reliable genetic testing. Our CR1 Gene CR1 deficiency Genetic Test provides valuable insights into an individual’s genetic makeup, allowing for personalized treatment and management strategies. Contact us today to schedule your test and take a step towards a healthier future.
| 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 o |
| Report Delivery | 3 to 4 Weeks |
| Method | NGS Technology |
| Test type | Neurological Disorders |
| Doctor | Neurologist |
| 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 |
| Test Details |
The CR1 gene encodes for the complement receptor 1 (CR1) protein, which plays a crucial role in regulating the complement system. CR1 deficiency is a rare genetic disorder characterized by a decrease or absence of CR1 protein on the surface of red blood cells and other cells in the body. This can lead to an overactive complement system, causing inflammation and damage to tissues. NGS (Next-Generation Sequencing) genetic testing is a type of DNA sequencing that allows for the analysis of multiple genes at once, providing a comprehensive view of an individual’s genetic makeup. NGS genetic testing can be used to diagnose CR1 deficiency by identifying mutations or variants in the CR1 gene. Genetic testing for CR1 deficiency may be recommended for individuals with a family history of the disorder or those experiencing symptoms such as recurrent infections, hemolytic anemia, or kidney disease. Early diagnosis and management of CR1 deficiency can help prevent complications and improve outcomes. |
