PRESENTATION OUTLINE
Phenylketonuria (PKU) is a rare condition in which a baby is born without the ability to properly break down an amino acid called phenylalanine.
Phenylketonuria (PKU) is inherited, which means it is passed down through families.
Untitled Slide
- Kids with pku often have lighter hair and lighter eyes than there siblings
Both parents must pass on the defective gene in order for a baby to have the condition
SYMPTOMS
- Seizures
- Skin rashes
- Tremors
- Hyperactivity