Journal of Obesity and Metabolism
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Paulus Blumberg
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Phenylketonuria (PKU) is a genetic metabolic disorder caused by a deficiency of the enzyme phenylalanine hydroxylase, leading to the accumulation of phenylalanine in the body. If left untreated, PKU can result in severe neurological impairment and cognitive deficits. This paper explores recent advancements in the management of PKU, focusing on diet... Read More»
: J Obes Metab 2024, 7:245
10.4172/jomb.1000245Abstract Peer-reviewed Full Article Peer-reviewed Article PDF Mobile Full Article
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