Question
What symptoms might a newborn experience if they have Phenylketonuria?
Answer
The diagnosis of Phenylketonuria typically requires further testing to confirm. If a newborn is suspected of having Phenylketonuria, the hospital will advise parents to bring the child in for a follow-up examination. During this waiting period, parents may feel worried and anxious. Phenylketonuria is a genetic metabolic disorder that may present with symptoms such as delayed intellectual development, growth retardation, abnormal skin and eye color, and an unusual body odor. These symptoms may not become apparent until the baby is older. It is important to adhere to medical treatment as prescribed to avoid long-term health issues.