英语词汇“phenylketonuria”的中英文释义、用法、翻译及短语词组-英汉翻译词典

phenylketonuria
- 英?[fen?lki:t?'nj??r??]
- 美?[?fen?l?kitn'j?r?fen?l?kitn'?ri?]
释义
n.
苯丙酮尿，苯丙酮酸尿症（一种先天性代谢异常）
大小写变形:Phenylketonuria
实用场景例句
- 全部
To explore the morbidity Congenital hypothyroidism ( CH ) and phenylketonuria ( PKU ) among newborn in Heze city.
了解菏泽市新生儿甲状腺功能低下症 ( CH ) 与苯丙酮尿症 ( PKU ) 发病率.
互联网
Separating Amino Acids in Blood and Urine by Microcrystalline Cellulose Film Chromatography - To ldentify Phenylketonuria.
硝酸纤维素薄膜在骨骼的α辐射自显影术方面的应用.
互联网
英英释义
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
行业词典
- 医学
  苯丙酮酸尿：一种由于苯丙氨酸羟化酶不足或缺陷造成的先天性代谢障碍，这种酶可将苯丙氨酸催化成酪氨酸???缺乏这种酶，使得苯丙氨酸及其代谢产物蓄积在体液中，除非以低苯丙氨酸的饮食治疗，否则可导致精神发育迟缓(苯丙酮酸性精神幼稚病)，有神经病状(包括运动过度、癫痫和小头畸形)、色素减少、湿疹和鼠臭味。本病为常染色体隐性遗传，缩写为PKU。典型苯丙酮酸尿有二种变型，轻微型病人可耐受饮食中较高含量的苯丙氨酸???短暂型只在婴幼儿期耐受性增高???
- 药学
  苯丙酮尿症???又称 :苯丙酮尿症(PKU )???

单词	phenylketonuria
释义	phenylketonuria 英?[fen?lki:t?'nj??r??] 美?[?fen?l?kitn'j?r?fen?l?kitn'?ri?] 释义 n. 苯丙酮尿，苯丙酮酸尿症（一种先天性代谢异常）大小写变形:Phenylketonuria 实用场景例句全部 To explore the morbidity Congenital hypothyroidism ( CH ) and phenylketonuria ( PKU ) among newborn in Heze city. 了解菏泽市新生儿甲状腺功能低下症 ( CH ) 与苯丙酮尿症 ( PKU ) 发病率. 互联网 Separating Amino Acids in Blood and Urine by Microcrystalline Cellulose Film Chromatography - To ldentify Phenylketonuria. 硝酸纤维素薄膜在骨骼的α辐射自显影术方面的应用. 互联网英英释义 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 行业词典医学苯丙酮酸尿：一种由于苯丙氨酸羟化酶不足或缺陷造成的先天性代谢障碍，这种酶可将苯丙氨酸催化成酪氨酸???缺乏这种酶，使得苯丙氨酸及其代谢产物蓄积在体液中，除非以低苯丙氨酸的饮食治疗，否则可导致精神发育迟缓(苯丙酮酸性精神幼稚病)，有神经病状(包括运动过度、癫痫和小头畸形)、色素减少、湿疹和鼠臭味。本病为常染色体隐性遗传，缩写为PKU。典型苯丙酮酸尿有二种变型，轻微型病人可耐受饮食中较高含量的苯丙氨酸???短暂型只在婴幼儿期耐受性增高??? 药学苯丙酮尿症???又称 :苯丙酮尿症(PKU )???
随便看	arthrogryposis cleft palate craniosynostosis arthrogryposis congenita arthrogryposis,congenital multiple arthrogryposis multiplex arthrogryposis multiplex congenita arthrogryposis multiplex congenital arthrogryposis syndrome arthrogrypotic arthroidal cartilage arthroidial cartilage arthrokatadesis arthrokatadysis arthrokleisis arthroklesis arthroleptid arthrolith arthrolithiasis Arthrologia arthrological arthrology arthrolysis Arthrolysis by stretching or manipulation arthromacra chifengi arthromacra formosana arthromacra minuta

phenylketonuria

释义

实用场景例句

英英释义

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

行业词典

医学

药学