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  2. Phenylketonuria - Wikipedia

    en.wikipedia.org/wiki/Phenylketonuria

    For a child to inherit PKU, both parents must have and pass on the defective gene. [17] If both parents are carriers for PKU, there is a 25% chance any child they have will be born with the disorder, a 50% chance the child will be a carrier and a 25% chance the child will neither develop nor be a carrier for the disease. [5]

  3. Hyperphenylalaninemia - Wikipedia

    en.wikipedia.org/wiki/Hyperphenylalaninemia

    Hyperphenylalaninemia most is commonly diagnosed by newborn screening and must be distinguished from classic PKU by confirmatory testing at an experienced center. Some cases in adult women have been detected using maternal screening programs or following birth of children with birth defects.

  4. 6-Pyruvoyltetrahydropterin synthase deficiency - Wikipedia

    en.wikipedia.org/wiki/6-Pyruvoyltetrahydropterin...

    It shares history with PKU and hyperphenylalaninemia (HPA) . Asbjørn Følling, a physician studying metabolic diseases, identified an excess of phenylpyruvate as the cause of a strange, musty odor from the urine of two Norwegian children. [13] Further research by Penrose in 1935 lead to the coining of the term, "phenylketonuria". The ...

  5. Inborn errors of metabolism - Wikipedia

    en.wikipedia.org/wiki/Inborn_errors_of_metabolism

    Disease involving amino acids (e.g. PKU, Tyrosinemia), organic acids, primary lactic acidosis, galactosemia, or a urea cycle disease 24 per 100,000 births [9] 1 in 4,200 [9] Lysosomal storage disease: 8 per 100,000 births [9] 1 in 12,500 [9] Peroxisomal disorder ~3 to 4 per 100,000 of births [9] ~1 in 30,000 [9] Respiratory chain-based ...

  6. 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 ...

  7. 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.

  8. 'The Crown's Leonora Knatchbull Was Only 5 Years Old When She ...

    www.aol.com/crowns-leonora-knatchbull-only-5...

    Leonora Knatchbull, 5, appears on the newest season of 'The Crown.' All about the little girl, Penny, and her relationship with her godmother, Princess Diana.

  9. 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 (PKU). [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]