Phenylketonuria is a genetic disorder characterized by abnormal levels of phenylalanine.

What is the normal value for phenylketonuria re-test?

Phenylketonuria is a congenital metabolic disorder that requires dietary control treatment to maintain normal values.

Phenylketonuria is a genetic disease that can be diagnosed and treated early through newborn screening to prevent complications.

The newborn phenylketonuria screening requires blood to be carefully examined through venipuncture.

Phenylketonuria is a genetic amino acid metabolic deficiency disease, with an autosomal recessive inheritance pattern.

The main newborn disease screenings include Phenylketonuria, Hypothyroidism, and Hearing. The results of the TSH and Phe tests are within the normal range, so you can rest assured that these screenings will not affect your baby’s intelligence. Hearing screening is also very important, but no relevant information was provided. It is recommended to consult a doctor for detailed interpretation. Overall, the baby’s screening results indicate no serious newborn diseases have been detected, and we wish the baby a healthy growth.

What should be the normal value for newborn phenylketonuria?

What symptoms might a baby with Phenylketonuria exhibit, and how should parents respond when they receive a positive test notification?

How to handle the situation after a child is misdiagnosed with Phenylketonuria for a year?