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To determine the level of G6PD in the blood, utilise the G6PD Quantitative.
Glucose-6-phosphate dehydrogenase, often known as G6PD, is a vital enzyme for the regular operation of red blood cells.
It is a component of blood required to deliver oxygen from the lungs to all cells.
This particular type of enzyme aids in adequately functioning red blood cells. Glucose-6-phosphate dehydrogenase deficiency happens when red blood cells are generally typically.
This can reduce hemolysis, which is essential for breaking down red blood cells. The most frequent cause of G6PD deficiency, in which red blood cells are lost more quickly is hemolytic anemia. The signs of hemolytic anemia in infants include pallor, icterus, jaundice, dark urine, palpitations, and shortness of breath.
Glucose 6-phosphate dehydrogenase deficiency is another important factor in severe jaundice in infants.
Glucose-6-phosphate dehydrogenase deficiency leads to mutations in the G6PD gene. This mutated gene provides instructions for the production of glucose-6-phosphate dehydrogenase. This enzyme will participate in the regular processing of carbohydrates.
Directions or medications such as sulfonamides, antimalarials, or blood thinners like aspirin may be to blame.
Palpitations are a sign of a glucose-6-phosphate dehydrogenase deficiency.
The G6PD range in a blood sample can be estimated using quantitative tests, yielding a G6PD activity result. Testing with numbers can provide precise measurements.
If a patient falls into the low or raised categories, this test can help determine that.
The technician will use a needle to draw blood from the arm's vein.
The results indicate a G6PD deficiency if they are lower.
| Test Type | Glucose 6-Phosphate Dehydrogenase (G6PD), Quantitative |
| Includes | Glucose 6-Phosphate Dehydrogenase G6PD Quantitative (Physician) |
| Preparation | |
| Reporting | Within 24 hours* |
| Test Price |
₹ 500
|
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