phenylketonuria
英：[fenəlki:tə'njʊərɪə] 美： [ˌfenəlˌkitn'jʊrˌfenəlˌkitn'ʊriə]
phenylketonuria 基本解释
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
phenylketonuria 相关例句
权威例句
PhenylketonuriaPhenylketonuriaPhenylketonuriaMonogenic traits are not simple: lessons from phenylketonuria.Neuropsychology of Early-Treated Phenylketonuria: Specific Executive Function DeficitsNeuropsychology of Early-treated Phenylketonuria: Specific Executive Function DeficitsMaternal 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.
