All proteins and some artificial sweeteners contain Phenylalanine in it Phenylketonuria. Your body. It is an inborn disorder, meaning it is developed and can be diagnosed at birth. Phenylketonuria is found more often in the Native American and Northern European ethnic groups backgrounds. It is less commonly observed in people from Asian, African, or Hispanic groups.
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Phenylketonuria: MedlinePlus Genetics
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The absence or deficiency of an enzyme, phenylalanine hydroxylase, that allows phenylalanine to accumulate in the blood and is toxic to brain tissue. Early detection and treatment is essential to prevent associated neurological symptoms. Without treatment, most infants develop mental retardation that is usually severe.
News Dr. March 11, Sleep Hygiene for Phenylketonuria If you or your child has phenylketonuria PKU , you may have trouble with sleep due to imbalances in signaling molecules in your body. If you Read more. March 4, March 4, Phenylketonuria and Sleep Phenylketonuria PKU is a rare metabolic disorder caused by mutations in a gene that cells use to make an enzyme.