Securing Future of Newborns with Neonatal G6PD Screening
Neonatal G6PD (glucose-6-phosphate dehydrogenase) deficiency is a genetic disorder that affects the red blood cells’ ability to function properly. It is one of the most common enzymatic deficiencies worldwide, particularly prevalent in populations with African, Mediterranean, Middle Eastern, and Southeast Asian ancestry. Early Detection of G6PD Deficiency in Newborns Early detection of G6PD deficiency in…