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  2. Phenylketonuria - Wikipedia

    en.wikipedia.org/wiki/Phenylketonuria

    PKU was the first disorder to be routinely diagnosed through widespread newborn screening. Robert Guthrie introduced the newborn screening test for PKU in the early 1960s. [67] With the knowledge that PKU could be detected before symptoms were evident, and treatment initiated, screening was quickly adopted around the world.

  3. Hyperphenylalaninemia - Wikipedia

    en.wikipedia.org/wiki/Hyperphenylalaninemia

    Phenylketonuria (PKU)-like symptoms, including more pronounced developmental defects, skin irritation, and vomiting, may appear when phenylalanine levels are near 20 mg/dL (1200 mol/L). [1] Hyperphenylalaninemia is a recessive hereditary metabolic disorder that is caused by the body's failure to convert phenylalanine to tyrosine as a result of ...

  4. Pleiotropy - Wikipedia

    en.wikipedia.org/wiki/Pleiotropy

    The blood of a two-week-old infant is collected for a PKU screening. A common example of pleiotropy is the human disease phenylketonuria (PKU). This disease causes mental retardation and reduced hair and skin pigmentation , and can be caused by any of a large number of mutations in the single gene on chromosome 12 that codes for the enzyme ...

  5. Her Daughter Will Never Be Able to Live Alone. So She ...

    www.aol.com/her-daughter-never-able-live...

    They then wanted to do a more in-depth panel because she has Phenylketonuria (PKU)," she explained. Along with further testing, they tried lifestyle changes in hopes of preventing seizures to get ...

  6. Neonatal heel prick - Wikipedia

    en.wikipedia.org/wiki/Neonatal_heel_prick

    The blood of a two-week-old infant is collected for a Phenylketonuria, or PKU, screening. The neonatal heel prick is a blood collection procedure done on newborns. It consists of making a pinprick puncture in one heel of the newborn to collect their blood. This technique is used frequently as the main way to collect blood from neonates.

  7. Inborn errors of metabolism - Wikipedia

    en.wikipedia.org/wiki/Inborn_errors_of_metabolism

    Another term used to describe these disorders is "enzymopathies". This term was created following the study of biodynamic enzymology , a science based on the study of the enzymes and their products. Finally, inborn errors of metabolism were studied for the first time by British physician Archibald Garrod (1857–1936), in 1908.

  8. Lofenalac - Wikipedia

    en.wikipedia.org/wiki/Lofenalac

    It is not recommended for non-PKU patients. [2] In 1972, Lofenalac was declared a food by the FDA, for regulatory purposes. [3] Initially the only available formula recommended was made by Mead Johnson. Others, including Albumaid XP, Cymogran, and Minafen, have since been developed in Britain. [4] Medical texts often recommend Lofenalac. [5] [6 ...

  9. European Society for Phenylketonuria and Allied Disorders ...

    en.wikipedia.org/wiki/European_Society_for...

    The E.S.PKU benchmark report [5] assesses the differences in care across Europe and provides a starting point for the E.S.PKU to improve any gaps in care that have been identified. [6] In consequence, the delegates decided that action is required to improve this situation. The report was presented [7] at the European Parliament. To underline ...