Tag: Phenylalanine free formula

Phenylketonuria (PKU) is a rare genetic disorder affecting approximately 1 in 10,000 to 15,000 newborns in the United States, identified through routine newborn screening. The recommended diet is a strict, lifelong low-protein eating plan that significantly restricts phenylalanine intake to prevent severe health consequences, especially brain damage.

According to the National Institutes of Health, a low phenylalanine diet is the primary treatment for managing phenylketonuria (PKU), a rare inherited disorder. A practical example of a low phenylalanine diet involves avoiding high-protein foods while relying on a special phenylalanine-free formula and carefully measured amounts of fruits, vegetables, and low-protein starches.

According to the European PKU guidelines, dietary management is essential for individuals with phenylketonuria to prevent intellectual disability and other severe complications. A cornerstone of this management is the strategic supplementation of vital nutrients that are restricted in a low-phenylalanine diet. Without these necessary supplements, a patient's health and development can be significantly compromised.

According to a study published in the *Orphanet Journal of Rare Diseases*, a strict, lifelong, low-phenylalanine diet is the principal treatment for Phenylketonuria (PKU). For infants, a specialized product is a core component of this management, raising the question: what is the PKU start formula, and how is it used?

In the United States, Phenylketonuria (PKU) affects about 1 in 25,000 newborns, making the need for a specific dietary regimen critical. A low phenylalanine diet is a lifelong medical nutrition therapy used to control this rare inherited disorder by restricting the intake of the amino acid phenylalanine.