Phenylketonuria is an amino acid metabolism disorder that primarily affects infants and young children. It is characterized by the inability of phenylalanine to be normally metabolized in the body, leading to its accumulation and potentially causing intellectual disability and other health issues. Treatment primarily involves dietary control to reduce the intake of phenylalanine, and may require rehabilitation training. Currently, there is no surgical treatment method.
This behavior can be normal in some infants, but it may sometimes be a sign of a hereditary metabolic disease. It is recommended to take your child to the hospital for a check-up.
Questions and Answers About Growing Pains
Whether a four-month-old baby can stand up and how to judge the baby’s health condition.
A child presents with diarrhea symptoms, initially diagnosed with chronic bronchitis, and after treatment shows improvement. However, diarrhea recurs. How should it be handled?
The duration of measuring body temperature and the normal temperature range
My baby developed jaundice a few days after birth. Now, a week has passed, and the jaundice has not subsided. Is this normal? How long does it take for newborn jaundice to disappear after it appears?
What should parents do if their newborn experiences seizures?
A nine-month-old child may experience sudden seizures at night due to high fever convulsions or potential epilepsy symptoms, and a Brain Electroencephalogram examination is necessary to determine the cause. For treatment, medications such as carbamazepine tablets, phenytoin sodium tablets, or diazepam can be used for adjustment.
What is the chemical substance indoleacetic acid in plants, and how does the hormone secreted by the anterior lobe of the pituitary gland affect height growth?
