phenylketonuria

听听怎么读
英 [fenəlki:tə'njʊərɪə]
美 [ˌfenəlˌkitn'jʊrˌfenəlˌkitn'ʊriə]
是什么意思
  • n.

    苯丙酮尿,苯丙酮酸尿症(一种先天性代谢异常);

  • 英英释义

    phenylketonuria[ 'fenil,ki:tə'njuri:ə, 'fi:- ]

    • n.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

      同义词:PKU

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    权威例句

    Phenylketonuria
    Phenylketonuria
    Phenylketonuria
    Monogenic traits are not simple: lessons from phenylketonuria.
    Neuropsychology of Early-Treated Phenylketonuria: Specific Executive Function Deficits
    Neuropsychology of Early-treated Phenylketonuria: Specific Executive Function Deficits
    Maternal phenylketonuria and hyperphenylalaninemia. An international survey of the outcome of untreated and treated pregnancies.
    A SIMPLE PHENYLALANINE METHOD FOR DETECTING PHENYLKETONURIA IN LARGE POPULATIONS OF NEWBORN INFANTS.
    Cell encapsulation as a potential nondietary therapy for maternal phenylketonuria.
    Hepatocyte nuclear factor 1 inactivation results in hepatic dysfunction, phenylketonuria, and renal Fanconi syndrome.
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