A five-year-old child with a metabolic disorder cannot walk, understands but cannot express, has congenital heart disease and developmental delays, seeking treatment advice.

Phenylketonuria is a common amino acid metabolism disorder that primarily affects infants. Early diagnosis followed by dietary treatment is crucial to prevent neurological damage.

Discusses the treatment of genetic metabolic disorders and potential complications.

Does a blood sugar level exceeding the normal range indicate diabetes?

What are the normal values for Phenylketonuria (PKU)?

Facial paralysis can be caused by a variety of factors, including infectious diseases, otorhinolaryngological diseases, Bell’s palsy, tumors, neurogenic conditions, traumatic injuries, poisoning (such as alcoholism, long-term exposure to toxic substances), metabolic disorders: such as diabetes, vitamin deficiency; vascular dysfunction, and congenital hypoplasia of the facial nerve nucleus.

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

How to treat phenylketonuria and the worst possible outcomes.

Phenylketonuria is a common amino acid metabolic disorder. When the PHE value in a newborn’s disease screening result is 2.37 too high, a re-examination is required. The earlier treatment begins, the better the outcome.