GPI Gene Hemolytic Anemia Nonspherocytic Genetic Test
Are you or your loved ones experiencing symptoms of hemolytic anemia? DNA Labs UAE offers a comprehensive genetic test to diagnose GPI gene hemolytic anemia nonspherocytic due to glucose phosphate isomerase deficiency. Our state-of-the-art NGS technology can identify any variations or mutations in the GPI gene, helping you understand the underlying cause of your condition.
Test Details
The GPI gene is responsible for producing an enzyme called glucose phosphate isomerase (GPI). Deficiency of this enzyme can lead to a type of hemolytic anemia called nonspherocytic hemolytic anemia. Our NGS genetic testing method analyzes the DNA sequence of the GPI gene, allowing us to identify any variations or mutations that may be causing the deficiency of the GPI enzyme.
By identifying the specific genetic mutation causing the deficiency, our NGS genetic testing can help diagnose individuals with nonspherocytic hemolytic anemia due to glucose phosphate isomerase deficiency. This information is crucial for proper treatment and management of the condition.
Test Components and Price
Our GPI Gene Hemolytic Anemia Nonspherocytic Genetic Test is priced at AED 4400.0. The test can be performed on a blood sample, extracted DNA, or even one drop of blood on an FTA card. We understand the importance of accurate and reliable results, which is why our laboratory utilizes NGS technology for precise genetic analysis.
Report Delivery and Test Department
Once the sample is received, our laboratory will process the test and deliver the report within 3 to 4 weeks. Our dedicated team of geneticists and medical professionals in the Genetics Department ensures that you receive accurate and comprehensive results.
Pre-Test Information and Genetic Counseling
Prior to undergoing the GPI Gene Hemolytic Anemia Nonspherocytic Genetic Test, it is important to provide a clinical history of the patient. Our General Physicians will also conduct a genetic counseling session to gather information and draw a pedigree chart of family members affected by hemolytic anemia due to glucose phosphate isomerase deficiency. This information helps in understanding the inheritance pattern and guiding future family planning decisions.
Conclusion
If you or your loved ones are experiencing symptoms of hemolytic anemia, our GPI Gene Hemolytic Anemia Nonspherocytic Genetic Test can provide valuable insights into the underlying cause. By identifying the specific genetic mutation causing the deficiency of the GPI enzyme, our NGS technology helps in accurate diagnosis and personalized treatment plans. Contact DNA Labs UAE today to schedule your genetic test and take a step towards better health.
Test Name | GPI Gene Hemolytic anemia nonspherocytic due to glucose phosphate isomerase deficiency Genetic Test |
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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 | Metabolic Disorders |
Doctor | General Physician |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for GPI Gene Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency |
Test Details |
The GPI gene is responsible for producing an enzyme called glucose phosphate isomerase (GPI). Deficiency of this enzyme can lead to a type of hemolytic anemia called nonspherocytic hemolytic anemia. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can be used to analyze the DNA sequence of the GPI gene. This test can identify any variations or mutations in the gene that may be causing the deficiency of the GPI enzyme. By identifying the specific genetic mutation causing the deficiency, NGS genetic testing can help diagnose individuals with nonspherocytic hemolytic anemia due to glucose phosphate isomerase deficiency. This information can also be useful for genetic counseling and family planning purposes. |