Neonatal G6PD Testing #EkSahiShuruat by Trivitron Healthcare

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…

Facts About Newborn Screening

Newborn screening is a crucial public health program that aims to identify genetic, metabolic, and congenital disorders in newborns. By conducting a simple blood test shortly after birth, healthcare professionals can detect these conditions early and initiate prompt treatment, preventing serious health complications and saving lives. In this piece of information, we will explore some…