Key Indicators Of Phenylketonuria

Delayed Development

A child who has phenylketonuria may experience delayed development as a direct result of the condition, or they may experience it due to the mother developing maternal phenylketonuria during her pregnancy. When a child has phenylketonuria at birth, their phenylalanine levels are normal. However, the levels of phenylalanine in the child's body will begin to rise within the first several hours after being born. If the child goes without treatment, cognitive delays will be apparent by the time the child reaches six months old. These delays precipitate from the toxicity of brain tissue caused by excessive levels of phenylalanine in the child's body. When the brain tissue becomes toxic, cellular damage will occur. The brain contains neurotransmitters or signaling molecules the cells utilize to communicate with each other. When certain neurotransmitters are not produced in the correct quantities, the brain is unable to function the way it should. High levels of phenylalanine cause impairment to the production of neurotransmitters vital for the child's learning, motivation, mood, and memory. Disruption in the normal process of any one of those aspects can result in delayed development in the affected child.

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