How Many Babies Have Galactosemia?

Galactosemia is a metabolic disorder that is genetically inherited in a recessive manner across generations in humans. Patients lack the 1-phosphogalactose uridylyltransferase enzyme, which prevents them from breaking down lactose from milk, leading to elevated levels of galactose in the blood and symptoms such as vomiting, liver enlargement, and cataracts.
One minute to read

How Pregnant Women Can Prevent Neonatal Jaundice

It is recommended that pregnant women enhance nutrition, maintain physical health, and consume more fruits and vegetables during pregnancy. At the same time, they should avoid taking medication and contracting infectious diseases such as colds and diarrhea. We should go to the hospital regularly for ultrasounds and other checks. If any abnormal issues are found, they should be addressed promptly. Generally, these measures can promote the normal development of the fetus.
One minute to read