Tag: Metabolic formula

According to the National Institutes of Health, a lifelong, meticulously planned dietary regimen is the primary treatment for phenylketonuria (PKU), a rare genetic disorder. This strict nutritional approach is essential for controlling phenylalanine levels, thereby preventing severe health complications, particularly intellectual disability. The role of nutrition in the management of phenylketonuria is central to patient well-being from infancy throughout adulthood.

According to the National Institutes of Health, phenylketonuria (PKU) is an inherited metabolic disorder affecting approximately 1 in every 10,000 to 15,000 newborns. The primary and lifelong treatment for this condition is a strict dietary intervention for PKU, which focuses on severely limiting the intake of the amino acid phenylalanine to prevent serious health complications.

Phenylketonuria (PKU) is a rare genetic disorder affecting approximately 1 in 25,000 newborns in the United States. It is caused by a gene mutation that results in the body's inability to properly process the amino acid phenylalanine, which is found in most dietary protein. This is why answering the question, "Can PKU drink milk?", is crucial for managing the condition and preventing serious health complications.