Case history
Case history
A full-term, female infant presents at 4 days of age with a positive newborn screening test for PKU. The history is unremarkable and physical exam reveals no abnormal findings. Plasma amino acid analysis shows a phenylalanine level of 20 mg/dL (normal levels are 1-2 mg/dL), with all other amino acids within normal ranges. Urine neopterin to biopterin ratio and blood dihydropteridine reductase activity are subsequently normal, ruling out a defect in tetrahydrobiopterin (BH4) synthesis or recycling.
Other presentations
Although in the US and other developed nations almost all patients with PKU are diagnosed through newborn screening, the same is not true in developing countries. If an adoptee from a developing nation should present with developmental delay, microcephaly, intellectual disability, or behavioral disturbances, the diagnosis of PKU should be considered. The presence of eczema may provide an additional clue. People >40 to 60 years of age were probably not screened at birth for PKU. Therefore, this diagnosis should also be ruled out in any patient with intellectual disability in this age group.
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