Newborn screenings include hypothyroidism, G6PD deficiency, phenylketonuria, congenital adrenal cortical insufficiency, and more. Hospitals will retain family contact information and notify immediately if results are abnormal. Families can also consult the neonatology department.

My child needs to undergo a medical examination. How is newborn disease screening conducted? Can you explain it in detail? Hello. Newborn heel prick blood test is a mandatory screening program and a means to detect related congenital diseases. Currently, our country mainly screens for congenital hypothyroidism and phenylketonuria. The heel prick blood is part of peripheral blood, making the blood collection relatively convenient. This has nothing to do with the exam results. Generally speaking, the exam results will be announced about a month later. If there are any abnormalities, further examination and clear diagnosis are required.

The baby has red spots and is vomiting. How can you determine if a newborn’s disease screening results are normal?

How to treat and control the blood phenylalanine concentration in children with phenylketonuria?

Newborns with polydactyly or webbed toes should undergo surgical treatment early to avoid future complications.

Treatment for Open Foramen Ovale in Newborns

If a newborn’s thyroid hormone levels are found to be low during disease screening, how should it be handled?

When a child is affected by newborn diseases, family members should seek medical treatment immediately, avoid blind medication, provide enough care and attention, and help treat the disease in a timely manner.

Treatment Methods and Medication Guidance for Newborn Jaundice

A newborn with hyoid osteogenesis imperfecta requires timely medical treatment.