Tag: Metabolic disorder management

The first successful dietary treatment for phenylketonuria (PKU) was developed in 1951, forever changing the prognosis for children born with this rare genetic disorder. The classical PKU diet is a strict, low-phenylalanine regimen that, when implemented shortly after birth, is crucial for preventing severe intellectual disability and other neurological complications. It remains the foundation of therapy for many individuals with PKU.

According to the National Institutes of Health, glutaric aciduria type 1 (GA-1) is a rare inherited metabolic disorder, and its management relies heavily on a specialized low-protein diet to reduce the accumulation of harmful substances. This means individuals must carefully monitor what foods should you avoid with glutaric aciduria to prevent serious neurological complications.