Phenylketonuria Index

Featured: Phenylketonuria Main Article

Phenylketonuria (PKU) is a disorder that is inherited. PKU disorder increases the levels of phenylalanine in the blood. Phenylalanine is an amino acid that is obtained through diet, and is found in some artificial sweeteners. Signs and symptoms of PKU may vary from mild to severe, and may include:

PKU has an autosomal recessive pattern of inheritance.

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Terms related to Phenylketonuria:

  • Deficiency Disease, Phenylalanine Hydroxylase
  • Folling Disease
  • Folling's Disease
  • PAH Deficiency
  • Phenylalanine Hydroxylase Deficiency Disease
  • PKU