phenylketonuria
英 [fenəlki:tə'njʊərɪə] 美 [ˌfenəlˌkitn'jʊrˌfenəlˌkitn'ʊriə]

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

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.