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The Swedish neonatal screening program effectively detects PKU, galactosaemia, and biotinidase deficiency with low false positives.

Pegvaliase effectively reduces blood phenylalanine levels in most PKU patients, but requires personalized plans and good communication to manage side effects.

Pegvaliase is recommended for treating adults with phenylketonuria.

Phenylalanine may help with depression but can cause issues if not properly processed.

Proper diet management is crucial for phenylketonuria patients to avoid severe health issues.