Non-Malaysian citizens are subject to 6% SST, to be verified and paid at the counter before screening.
G6PD deficiency (Glucose-6-Phosphate Dehydrogenase Deficiency) is a common inherited enzyme disorder affecting red blood cells. Without sufficient G6PD enzyme, red cells may break down (hemolysis) when exposed to certain drugs, infections, or foods (such as fava beans). Newborn screening is strongly recommended.
A blood test is performed to measure G6PD enzyme activity. In newborns, heel-prick blood samples are commonly used for quick screening.
Q1: What are the symptoms of G6PD deficiency?
A: Common signs include newborn jaundice, acute hemolysis (fever, dark urine, anemia, fatigue).
Q2: Can G6PD deficiency be cured?
A: There is no cure, but by avoiding triggers (certain drugs, foods, infections), individuals can live a healthy life.
Q3: Which foods or drugs should be avoided?
A: Typical examples include fava beans, sulfa drugs, and high-dose aspirin. Doctors will provide specific guidance.