Treatment and prevention measures for phenylketonuria detected in 15-day-old infants

The mode of inheritance for phenylketonuria, based on inheritance across generations, is primarily managed through dietary treatment.

What is Phenylketonuria and what are the criteria for a positive result?

FAQs and Answers About Phenylketonuria

Phenylketonuria patients have specific dietary restrictions. This article provides relevant questions and answers.

Which hospital in Beijing offers the best treatment outcomes for patients with phenylketonuria?

Special dietary treatment methods for phenylketonuria patients

Understanding the symptoms of phenylketonuria, including intellectual development delay, seizures, and growth delay, as well as how to observe them in infancy.

Understanding the symptoms of phenylketonuria, including delayed intellectual development, seizures, and abnormal behavior, as well as parental concerns about genetic risks and early identification in newborns.

The symptoms of pediatric phenylketonuria mainly manifest as abnormal body odor and digestive problems, caused by an abnormal metabolism of phenylalanine in the body. Treatment primarily involves dietary control, limiting the intake of phenylalanine, and increasing the intake of fats and nutrients.