G6PD (glucose-6-phosphate dehydrogenase) is an enzyme crucial for protecting red blood cells from oxidative damage. lt plays a key role in the pentose phosphate pathway, maintaining NADPH levels that safeguard cells. G6PD deficiency is a commonX-linked genetic disorder, especially prevalent in males from Africa, Asia and the Medi-terranean. When exposed to certain triggers, such as specific medications, infections or fava beans - affected individuals can experience acute hemolysis, leading to anemia, jaundice and dark urine. There is no cure, but avoiding triggers allows most people to live normally.

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