The Prevalence of Phenylketonuria in Arab Countries, Turkey, and Iran: A Systematic Review.

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phenylketonuria 6 endocrinologydiseases

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phenylketonuria 2642 deficient) are thought to be heterogeneous disorders that vary from severe, for example, classical phenylketonuria (PKU), to mild, benign, and transient forms. Enzyme deficiency yields a spectrum of disorders such as
phenylketonuria 2793 transient forms. Enzyme deficiency yields a spectrum of disorders such as mild hyperphenylalaninemia, mild phenylketonuria , and classic phenylketonuria. Classic phenylketonuria is a result of near complete or complete deficiency
phenylketonuria 2822 yields a spectrum of disorders such as mild hyperphenylalaninemia, mild phenylketonuria, and classic phenylketonuria . Classic phenylketonuria is a result of near complete or complete deficiency of phenylalanine hydroxylase
phenylketonuria 2847 disorders such as mild hyperphenylalaninemia, mild phenylketonuria, and classic phenylketonuria. Classic phenylketonuria is a result of near complete or complete deficiency of phenylalanine hydroxylase activity which will
phenylketonuria 3114 disability in the absence of dietary restriction of phenylalanine. Mild hyperphenylalaninemia and mild phenylketonuria are linked to a lower risk of impaired cognitive development if left untreated [[2]]. All of the aforementioned
phenylketonuria 3704 seizures, and an incapability to control body temperature.Today, the clinical manifestations of classic phenylketonuria are rarely reported in the developed countries, where newborn screening (NBS) is prevalent. NBS has

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