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.

The Anti-Phospholipid Antibody Test detects antibodies against phospholipids, helping diagnose antiphospholipid syndrome (APS) and assess the risk of blood clots.

A blood sample is collected from a vein in your arm and analyzed for the presence of antiphospholipid antibodies.

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

Results are usually available within 1-2 days, depending on the laboratory’s processing time.

Discuss any abnormal results with your healthcare provider, who will guide you on further tests or treatment options based on your specific condition.

Types include open prostatectomy, laparoscopic prostatectomy, robotic-assisted laparoscopic prostatectomy, and transurethral resection of the prostate (TURP).