Phenylketonuria is an amino acid metabolism disorder, with treatment focusing on early diagnosis and dietary therapy.

Appropriateness of drinking whey protein powder containing phenylalanine during pregnancy

Methods for diagnosing and preventing phenylketonuria

What dietary considerations should phenylketonuria patients be aware of?

Understand the relationship between newborn jaundice and PHE values and their treatment methods.

Phenylketonuria is a genetic disorder with an autosomal recessive inheritance pattern.

Suggestions for Handling Phenylketonuria Screening Failure in Newborns

How to prepare a suitable diet plan for a 5-year-old phenylketonuria patient

How long do children with phenylketonuria live?

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