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.

Protein S is a protein that helps regulate blood clotting by assisting in the deactivation of clotting factors and promoting the breakdown of clots. Its proper function is crucial for preventing abnormal clot formation and related disorders.

A blood sample is drawn from a vein in your arm. The sample is then analyzed to measure Protein S levels and activity.

No fasting or special preparation is required before the test. You can eat and drink as usual.

Results are typically available within a few hours to 1-2 days, depending on the laboratory’s processing time.

If your results are abnormal, your healthcare provider will discuss them with you and may recommend additional tests or adjustments to your treatment plan based on your specific condition.

Fasting helps obtain accurate measurements of cholesterol and triglyceride levels.