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little is known about these additional genetic factors. It works by increasing your tolerance to phenylalanine. Classic PKU, the most severe form of the disorder, occurs when phenylalanine hydroxylase activity is severely reduced or absent. Additional NIH Resources (2 links educational Resources (9 links patient Support and Advocacy Resources (7 links). Formula for people with PKU, because of the restricted diet, people with PKU need to get essential nutrients through a special nutritional supplement. Your doctor and dietitian can help you find the right type of formula. Plan ahead when you eat out. If PKU is not treated, phenylalanine can build up to harmful levels in the body, causing intellectual disability and other serious health problems.
Back to Home Does, pKU happen more frequently in a certain ethnic group?
Ask your doctor or dietitian if there are programs or insurance plans that help cover the high costs of formula and low-protein foods. Infants with classic PKU appear normal until they are a few months old. Learn more about autosomal recessive inheritance. Babies born to mothers who have PKU and uncontrolled phenylalanine levels (women who no longer follow a low-phenylalanine diet) have a significant risk of intellectual disability because they are exposed to very high levels of phenylalanine before birth. Socialstyrelsens riktlinjer kan delas i fyra kategorier. The test is done after your baby is 24 hours old and after your baby has ingested some protein in the diet to ensure accurate migrationsverket malmö öppettider results. Maintain a positive food attitude. These strategies may help: Stay informed. High amounts phenylalanine in the blood might indicate that your baby has PKU. A safe amount of phenylalanine differs for each person with PKU and can vary over time.
Are there any medications to treat this disease? Genetic and Rare Diseases Information Center (1 link).