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G6PD Gene Hemolytic Anemia Due to G6PD Deficiency Genetic Test Cost

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

-21%

The G6PD Gene Hemolytic Anemia Due to G6PD Deficiency Genetic Test is a diagnostic procedure aimed at identifying individuals with Glucose-6-Phosphate Dehydrogenase (G6PD) deficiency, a genetic condition that can lead to hemolytic anemia. This condition arises when the body lacks enough G6PD enzyme, which is crucial for the normal processing of red blood cells. Without sufficient G6PD, red blood cells can be destroyed prematurely, leading to anemia.

This test specifically searches for mutations in the G6PD gene, which are indicative of the deficiency. It’s a vital tool for diagnosing individuals who exhibit symptoms of G6PD deficiency or those who are at risk due to their family history. Symptoms can range from fatigue and jaundice to severe cases of anemia triggered by infections, certain foods, or medications.

Conducted at DNA Labs UAE, the test is priced at 4400 AED. The process involves collecting a blood sample from the individual, which is then analyzed in the laboratory for genetic markers of G6PD deficiency. The results of this test can provide crucial information for managing the condition, including guidance on avoiding certain triggers and insights into the risk of passing the deficiency on to offspring. This genetic test is a cornerstone in the proactive management of G6PD deficiency, offering individuals and their families the means to better understand and navigate this genetic condition.

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G6PD Gene Hemolytic Anemia Due to G6PD Deficiency Genetic Test

At DNA Labs UAE, we offer the G6PD Gene Hemolytic Anemia Due to G6PD Deficiency Genetic Test at a cost of AED 4400.0. This test is used to diagnose and manage G6PD deficiency, a condition caused by a deficiency of the G6PD enzyme.

Test Details

G6PD (glucose-6-phosphate dehydrogenase) gene hemolytic anemia is a condition caused by a deficiency of the G6PD enzyme. This enzyme plays a crucial role in protecting red blood cells from oxidative damage. Without enough G6PD, red blood cells become more susceptible to destruction, leading to hemolytic anemia.

NGS (next-generation sequencing) genetic testing is a technique used to analyze multiple genes simultaneously, including the G6PD gene. This test can identify mutations or variations in the G6PD gene that may cause a deficiency in the G6PD enzyme. By identifying specific genetic variations, NGS testing can help diagnose G6PD deficiency and determine the severity of the condition. It can also provide information about the risk of hemolytic anemia and guide treatment decisions.

NGS genetic testing is often recommended for individuals with a family history of G6PD deficiency or those who have experienced symptoms of hemolytic anemia. It can also be used for carrier screening in certain populations with a higher prevalence of G6PD deficiency.

Overall, NGS genetic testing for G6PD gene hemolytic anemia is a valuable tool for diagnosing and managing this condition, allowing for personalized treatment plans and genetic counseling.

Test Components and Price

  • Test Name: G6PD Gene Hemolytic Anemia Due to G6PD Deficiency Genetic Test
  • Components: Blood or Extracted DNA or One drop Blood on FTA Card
  • Price: AED 4400.0

Report Delivery

The report for the G6PD Gene Hemolytic Anemia Due to G6PD Deficiency Genetic Test will be delivered within 3 to 4 weeks.

Method

The G6PD Gene Hemolytic Anemia Due to G6PD Deficiency Genetic Test utilizes NGS (next-generation sequencing) technology.

Test Type

The G6PD Gene Hemolytic Anemia Due to G6PD Deficiency Genetic Test falls under the category of metabolic disorders.

Doctor

This test can be ordered by a general physician.

Test Department

The G6PD Gene Hemolytic Anemia Due to G6PD Deficiency Genetic Test is conducted in our Genetics department.

Pre Test Information

Prior to undergoing the G6PD Gene Hemolytic Anemia Due to G6PD 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 by Hemolytic Anemia due to G6PD deficiency.

Don’t wait any longer! Get the G6PD Gene Hemolytic Anemia Due to G6PD Deficiency Genetic Test at DNA Labs UAE today and take control of your health.

Test Name G6PD Gene Hemolytic anemia due to G6PD 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 Metabolic Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for G6PD Gene Hemolytic anemia due to G6PD deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Hemolytic anemia due to G6PD deficiency
Test Details

G6PD (glucose-6-phosphate dehydrogenase) gene hemolytic anemia is a condition caused by a deficiency of the G6PD enzyme. This enzyme plays a crucial role in protecting red blood cells from oxidative damage. Without enough G6PD, red blood cells become more susceptible to destruction, leading to hemolytic anemia.

NGS (next-generation sequencing) genetic testing is a technique used to analyze multiple genes simultaneously, including the G6PD gene. This test can identify mutations or variations in the G6PD gene that may cause a deficiency in the G6PD enzyme.

By identifying specific genetic variations, NGS testing can help diagnose G6PD deficiency and determine the severity of the condition. It can also provide information about the risk of hemolytic anemia and guide treatment decisions.

NGS genetic testing is often recommended for individuals with a family history of G6PD deficiency or those who have experienced symptoms of hemolytic anemia. It can also be used for carrier screening in certain populations with a higher prevalence of G6PD deficiency.

Overall, NGS genetic testing for G6PD gene hemolytic anemia is a valuable tool for diagnosing and managing this condition, allowing for personalized treatment plans and genetic counseling.