G6PD deficiency is a genetic disorder that affects the red blood cells, making them more vulnerable to breaking down prematurely.

Symptoms such as fatigue, jaundice, dark urine, or a family history of G6PD deficiency may indicate the need for this test.

The G6PD test is a simple blood test with minimal risks, similar to any standard blood draw.

Management includes avoiding triggers such as certain medications, foods, and infections that can cause hemolysis.

Early detection in newborns can prevent severe jaundice and related complications by guiding appropriate care and dietary adjustments.

Hospital stay typically ranges from a few days to a week, depending on the complexity of the surgery and your recovery progress.

Symptoms may include fatigue, weakness, shortness of breath, irritability, and tongue changes.

Treatment involves folic acid supplementation through oral tablets or injections, depending on the severity of the deficiency.

Yes, diets low in leafy greens, fruits, and fortified cereals may lead to folic acid deficiency.

Frequency depends on individual risk factors and health conditions. Consult your healthcare provider for personalized advice.

The test involves a simple blood draw with minimal risks, such as slight bruising at the puncture site.