PKU

NOUN
  1. a genetic disorder of metabolism; lack of the enzyme needed to turn phenylalanine into tyrosine results in an accumulation of phenylalanine in the body fluids which causes various degrees of mental deficiency
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How To Use PKU In A Sentence

  • (Unless you have a genetic disease called phenylketonuria (PKU), which prevents you from digesting the amino acid phenylalanine. Dr. Joseph Mercola: The Deadly Neurotoxin Nearly EVERYONE Uses Daily (VIDEO)
  • It would be another quarter of a century before scientists finally identified Carol’s condition she was suffering from phenylketonuria, or PKU, brain degeneration caused by inability in the newborn child to process a chemical called phenyl, a deficiency that can be treated only if detected in its early stages. PEARL BUCK IN CHINA
  • Feb. 26th, 2004: Princess Maha Chakri·Sirindhorn of the Kingdom of Thailand visited PKU. The vice president of PKU Hao Ping met the visitor.
  • These conditions include sickle cell anemia, beta thalassemia, phenylketonuria PKU, hypothyroidism,8 and galactosemia. Pregnancy, Childbirth, and the Newborn
  • Virtually the only people who cannot consume the artificial sweetener aspartame are those who have a rare hereditary disease called phenylketonuria PKU—and every product that contains aspartame carries a PKU warning on the label. The Small Change Diet
  • As an example of the power of environmental effects, consider infants with the genetic disorder PKU (phenylketonuria). The Volokh Conspiracy » Some Scientists’ Openness to the Possibility of Genetic Differences in Mental Traits Among Racial and Ethnic Groups
  • I must here also mention a simple little instrument called _keipkūttuk_, being a slender rod of bone nicely rounded, and having a point at one end and a knob or else a laniard at the other. Journal of the Third Voyage for the Discovery of a North-West Passage
  • Years ago all babies were screened for a very rare condition called phenylketonuria PKU with a blood test. The Official Lamaze® Guide
  • PKU is described by scientists as an autosomal recessive genetic disease that is characterized by a deficiency in an enzyme called phenylalanine hydroxylase (PAH). Medlogs - Recent stories
  • The three main laboratory methods used to screen newborns for PKU are the Guthrie bacterial inhibition assay, fluorometric analysis and tandem mass spectrometry.
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