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GPI Gene Hemolytic Anemia Nonspherocytic Due to Glucose Phosphate Isomerase Deficiency Genetic Test Cost

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

-21%

GPI Gene Hemolytic Anemia Nonspherocytic due to Glucose Phosphate Isomerase Deficiency is a rare genetic disorder affecting the red blood cells. This condition is characterized by the body’s inability to properly produce glucose phosphate isomerase, an enzyme essential for the glycolytic pathway, leading to nonspherocytic hemolytic anemia. Symptoms can vary from mild to severe and may include fatigue, jaundice, an enlarged spleen, and increased susceptibility to infections.

To diagnose this condition, a genetic test targeting the GPI gene can be performed. This test identifies mutations in the GPI gene that are responsible for the enzyme deficiency. DNA Labs UAE offers this specific genetic testing service for individuals suspected of having this rare disorder. The cost of the test is 4400 AED. This comprehensive testing can be crucial for accurate diagnosis, allowing for appropriate management and treatment strategies to be implemented for those affected by this condition.

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GPI Gene Hemolytic Anemia Nonspherocytic Due to Glucose Phosphate Isomerase Deficiency Genetic Test

At DNA Labs UAE, we offer the GPI Gene Hemolytic Anemia Nonspherocytic Due to Glucose Phosphate Isomerase Deficiency Genetic Test. This test is designed to diagnose individuals suspected of having hemolytic anemia due to glucose phosphate isomerase deficiency.

Test Details

The GPI gene is responsible for producing an enzyme called glucose phosphate isomerase (GPI). Hemolytic anemia refers to a condition where red blood cells are destroyed faster than they can be replaced, leading to a shortage of healthy red blood cells. Nonspherocytic anemia means that the red blood cells are not abnormally shaped (as is the case in spherocytic anemia). Glucose phosphate isomerase deficiency is a rare genetic disorder that results from mutations in the GPI gene. These mutations lead to reduced or absent GPI enzyme activity, which is essential for the normal function of red blood cells. Without sufficient GPI enzyme activity, red blood cells are more prone to destruction, leading to hemolytic anemia.

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

Before undergoing the GPI Gene Hemolytic Anemia Nonspherocytic Due to Glucose Phosphate Isomerase Deficiency Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected with GPI Gene Hemolytic Anemia Nonspherocytic Due to Glucose Phosphate Isomerase Deficiency.

Test Method

NGS (Next-Generation Sequencing) genetic testing is used to analyze the DNA sequence of an individual’s genes. This technique can identify specific mutations or variants in the GPI gene associated with glucose phosphate isomerase deficiency. NGS genetic testing allows for the detection of a wide range of genetic variations quickly and efficiently.

Importance of the Test

By performing NGS genetic testing on an individual suspected of having hemolytic anemia due to glucose phosphate isomerase deficiency, healthcare professionals can confirm the diagnosis and provide appropriate treatment and management strategies. Early detection and intervention can greatly improve the quality of life for individuals with this genetic disorder.

For more information or to schedule an appointment for the GPI Gene Hemolytic Anemia Nonspherocytic Due to Glucose Phosphate Isomerase Deficiency Genetic Test, please contact DNA Labs UAE.

Test Name GPI Gene Hemolytic anemia nonspherocytic due to glucose phosphate isomerase 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 Hematology
Doctor Hematologist
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 GPI Gene Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency NGS Genetic DNA Test gene GPI
Test Details

The GPI gene is responsible for producing an enzyme called glucose phosphate isomerase (GPI). Hemolytic anemia refers to a condition where red blood cells are destroyed faster than they can be replaced, leading to a shortage of healthy red blood cells. Nonspherocytic anemia means that the red blood cells are not abnormally shaped (as is the case in spherocytic anemia).

Glucose phosphate isomerase deficiency is a rare genetic disorder that results from mutations in the GPI gene. These mutations lead to reduced or absent GPI enzyme activity, which is essential for the normal function of red blood cells. Without sufficient GPI enzyme activity, red blood cells are more prone to destruction, leading to hemolytic anemia.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze the DNA sequence of an individual’s genes. It can identify specific mutations or variants in the GPI gene associated with glucose phosphate isomerase deficiency. This testing method allows for the detection of a wide range of genetic variations quickly and efficiently.

By performing NGS genetic testing on an individual suspected of having hemolytic anemia due to glucose phosphate isomerase deficiency, healthcare professionals can confirm the diagnosis and provide appropriate treatment and management strategies.