Children with phenylketonuria may exhibit symptoms of delayed growth and development, language disorders, and other issues after the age of 1. The key to treatment lies in controlling the content of phenylalanine in their diet.
The diagnostic success rate of phenylketonuria is relatively low, and timely treatment is necessary. Parents should also avoid taking their children to crowded places to prevent the deterioration of the disease.
The Treatment Period and Main Clinical Manifestations of Phenylketonuria
Phenylketonuria is a common genetic amino acid metabolism disorder characterized by intellectual disability and neurological symptoms.
Phenylketonuria is a congenital disease that cannot be cured, but with proper treatment and dietary control, symptoms can be alleviated and the patient’s quality of life can be improved.
Information on the treatment and prognosis of neonatal phenylketonuria diagnosed within 14 days.
Neonatal phenylketonuria, as a genetic metabolic disorder, although with a low incidence rate, timely treatment is crucial for the improvement of the condition.
Treatment recommendations and precautions for neonates with phenylketonuria
Explore the treatment methods for phenylketonuria, emphasizing the importance of early diagnosis and dietary therapy.
What are the treatment options for phenylketonuria?
