Tag: High phenylalanine

Affecting approximately 1 in 12,000 newborns in the United States, phenylketonuria (PKU) is a rare genetic disorder that is the most common cause of excess phenylalanine. When the body is unable to properly metabolize this amino acid, it can build up to toxic levels, damaging the brain and causing a host of other serious health issues.

Phenylketonuria (PKU) is a rare genetic disorder that affects approximately 1 in 10,000 to 15,000 newborns in the United States. This condition prevents the body from properly processing the amino acid phenylalanine (Phe), and understanding the symptoms of too much phenylalanine is crucial for managing the condition and preventing severe health issues.

Did you know that in the U.S., approximately 1 in 25,000 newborns are diagnosed with phenylketonuria (PKU), a rare genetic disease? For those with this condition, learning how to get phenylalanine out of your system—or more accurately, manage its levels—is crucial for preventing serious lifelong health complications.

According to research from MedlinePlus Genetics, the accumulation of high levels of the amino acid phenylalanine is often linked to the inherited disorder phenylketonuria (PKU). This condition primarily manifests in those with a genetic inability to process phenylalanine effectively, leading to potentially toxic levels that can significantly harm the brain and nervous system.