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Phenylketonuria (commonly known as PKU) is an inherited disorder that increases the levels of a substance called phenylalanine in the blood. Phenylalanine is a building block of proteins (an amino
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Phenylketonuria (PKU) is a rare inherited disorder that causes an amino acid called phenylalanine to build up in the body. PKU is usually detected through newborn screening. Oformr is a form used for reporting PKU cases and treatment.
Healthcare providers and laboratories are required to file the phenylketonuria disorder and oformr.
The phenylketonuria disorder and oformr can be filled out with the necessary patient information, test results, and follow-up treatment plans.
The purpose of the phenylketonuria disorder and oformr is to track and monitor cases of PKU, ensure appropriate treatment is provided, and comply with reporting requirements.
Information such as patient demographics, test results, treatment plans, and follow-up monitoring must be reported on the phenylketonuria disorder and oformr.
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