GPI Gene Hemolytic Anemia Nonspherocytic Due to Glucose Phosphate Isomerase Deficiency NGS Genetic DNA Test
Introduction
The GPI Gene Hemolytic Anemia Nonspherocytic Due to Glucose Phosphate Isomerase Deficiency NGS Genetic DNA Test is a vital diagnostic tool used to identify genetic mutations that lead to nonspherocytic hemolytic anemia. This condition is characterized by the premature destruction of red blood cells, leading to various health complications. Understanding your genetic makeup can provide insights into your health and guide appropriate treatment options.
What the Test Measures
This test employs Next-Generation Sequencing (NGS) technology to detect mutations in the GPI gene, which is responsible for encoding the enzyme glucose phosphate isomerase. Deficiencies in this enzyme can lead to metabolic disturbances and hemolytic anemia.
Who Should Consider This Test
Individuals who experience symptoms such as fatigue, jaundice, or dark urine may benefit from this test. Additionally, those with a family history of hemolytic anemia or related metabolic disorders should consider undergoing genetic testing to determine their risk factors.
Benefits of Taking the Test
- Early detection of GPI deficiency.
- Informed decision-making regarding treatment options.
- Understanding of hereditary risks for family members.
- Access to tailored management strategies for hemolytic anemia.
Understanding Your Results
Results from the GPI Gene Hemolytic Anemia Nonspherocytic Test will indicate whether mutations are present. A genetic counseling session is recommended to discuss the implications of your results, including potential treatment pathways and family planning considerations.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| GPI Gene Hemolytic Anemia Nonspherocytic NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book Your Test Today!
Don’t wait to take charge of your health. Book the GPI Gene Hemolytic Anemia Nonspherocytic Due to Glucose Phosphate Isomerase Deficiency NGS Genetic DNA Test today! For inquiries or to schedule your appointment, call or WhatsApp us at +2348077798758.
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One Drop Blood on FTA Card
Pre-Test Instructions: A clinical history of the patient is required, along with a genetic counseling session to draw a pedigree chart of family members affected with hemolytic anemia.
Specialty and Department
This test falls under the specialty of General Physician and the department of Genetics, utilizing NGS Technology to diagnose Metabolic Disorders.
