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Peterchris Okpala
Dr, Department of Chanchellor’s Office, Charisma University, Providenciales, Turks and Caicos Islands
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Review
Management of Phenylketonuria
Author(s): Peterchris Okpala*
Phenylketonuria is among the most prevalent amino acid deficiency diseases that affect Americans. Phenylketonuria is an inherited amino acid deficiency disease that causes increased phenylalanine levels, a building block of proteins, in the blood. The condition is prevalent in the United States as it occurs in one out of 10,000 or 15,000 births. Persons with phenylketonuria experience psychiatric disorders, intellectual disability, hyperactivity, behavioral problems, eczema, and neurological issues. A significant percentage of individuals with phenylketonuria do not receive evidence-based care in the United States. Persons with phenylketonuria experience neurological signs, recurrent headaches, tremors, and seizures for failing to complete comprehensive treatment. The research aims to provide detailed information on evidence-based treatment and prevention methods.. View more»