Neonatal disease testing cannot detect white matter malnutrition, which is mainly used for detecting genetic diseases.

Neonatal galactosemia is typically curable; parents are advised to take their child to the doctor as soon as possible and follow medical instructions for treatment.

Neonatal hardening often occurs in premature infants, affected by cold and inadequate warming, which can lead to difficulty breathing and circulatory failure in severe cases, even resulting in death.

A newborn developed a rash on the hand 40 days after birth, diagnosed as a capillary hemangioma. This article discusses whether treatment is necessary and its potential impact on the infant.

Inquire about the treatment and sequelae of neonatal hemolytic disease.

Treatment Methods and Prognosis of Neonatal Hemolytic Disease

Neonatal hemolytic disease can be improved through timely medical treatment, including phototherapy, medication, and dialysis therapy.

Neonatal hemolytic disease has the potential to self-heal, but requires close observation and appropriate treatment.

Neonatal hemolytic disease is an autoimmune response caused by incompatibility between the mother’s and the newborn’s blood types. The condition can be relieved through treatments such as blue light therapy, blood transfusion, and medication.

Neonatal jaundice is a common phenomenon, but the risk can be reduced by paying attention to the mother’s diet during pregnancy and ensuring adequate nutrition intake.