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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. Pegvaliase - Wikipedia

    en.wikipedia.org/wiki/Pegvaliase

    Pegvaliase, sold under the brand name Palynziq, is a medication used for the treatment of the genetic disease phenylketonuria. [5] [9] [10] It is a phenylalanine (Phe)‑metabolizing enzyme. [5] Chemically, it is a pegylated derivative of the enzyme phenylalanine ammonia-lyase that metabolizes phenylalanine to reduce its blood levels. [5]

  4. 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 ...

  5. Tetrahydrobiopterin deficiency - Wikipedia

    en.wikipedia.org/wiki/Tetrahydrobiopterin_deficiency

    Tetrahydrobiopterin is a cofactor in the production of L-DOPA from tyrosine and 5-hydroxy-L-tryptophan from tryptophan, which must be supplemented as treatment in addition to the supplements for classical PKU. [citation needed] Other underlying causes of tetrahydrobiopterin deficiency are: [2] 6-Pyruvoyltetrahydropterin synthase (PTPS) deficiency

  6. Some say too many transgender kids are given hormones. Data ...

    www.aol.com/news/too-many-transgender-kids-given...

    A new study found less than .1% of transgender and gender-diverse teens are prescribed puberty blockers or gender-affirming hormones.

  7. 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 ...

  8. Rock & Roll Hall of Fame Achieves Its Biggest Induction ...

    www.aol.com/rock-roll-hall-fame-achieves...

    The Rock & Roll Hall of Fame induction ceremony also improved its rating among the key adults age 18-49 demographic, nabbing a 0.5 — up 39% from the 0.36 achieved in 2023, and tying the show’s ...

  9. Billy Crystal and Wife Janice Reveal Their Home of 46 Years ...

    www.aol.com/billy-crystal-wife-janice-reveal...

    Billy Crystal and his wife, Janice Crystal's home has been destroyed by the deadly Los Angeles wildfires.. The celebrated actor confirmed in a statement to PEOPLE that the couple's home in the ...