Importance of early detection of phenylketonuria in neonates
DOI:
https://doi.org/10.35381/s.v.v8i1.3846Keywords:
Phenylketonurias, phenylketonuria maternal, prolidase deficiency, (Source: DeCS)Abstract
Objective: To analyze the importance of early detection of phenylketonuria in neonates. Method: Descriptive documentary. Conclusion: Phenylketonuria is a pathology caused by a metabolic error due to the lack of functionality of phenylalanine hydroxylase, since the body does not properly synthesize this essential amino acid to form tyrosine. Not having an adequate control causes high levels of phenylalanine in the body triggering damage to the central nervous system resulting in brain pathologies, this disease is also determined as congenital because it can be inherited being the parents their carriers.
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