Phenylketonuria

英音[ ˌfiːnaɪlˌkiːtəˈnjʊərɪə; ˌfenaɪlˌkiːtəˈnjʊərɪə ] 美音[ ˌfenəlˌkiːtnˈ(j)ʊriə; ˌfiːnəlˌkiːtnˈ(j)ʊriə ]

[泌尿] 苯丙酮尿

常用释义

n. [泌尿] 苯丙酮尿；[泌尿] 苯丙酮酸尿

扩展信息

苯酮尿症

9，苯酮尿症（phenylketonuria）：是由于苯丙氨酸羟化酶缺乏引起苯丙酸堆积的代谢遗传病。缺乏丙酮酸羟化酶，苯丙氨酸只 …

苯丙酮尿症

PKU 苯丙酮尿症（phenylketonuria）的缩写，一种遗传病，其症状是尿中出现超出常规水平的苯丙酮酸。普通登录手机登录 …

苯丙酮酸尿症

（八）苯丙酮酸尿症（phenylketonuria）　本症是遗传代谢缺陷所致智力低下中较常见的类型，1934年由Folling首先描述，故又 …

苯丙胺尿症

　　（二）苯丙胺尿症（phenylketonuria）本病主要因先天性酶缺陷，不能将苯丙胺酸转化，因而在体内积聚所致。是一种常染色 …

苯丙酮酸尿毒症

对乙酰半胱氨酸过敏者禁用；因本品含有甜味剂阿司巴甜（aspartame），苯丙酮酸尿毒症(phenylketonuria)患者禁用。注意事 …

苯酮酸尿症

儿科常用护理英语词汇精选 ... Parasitic infestation 寄生虫感染 Phenylketonuria 苯酮酸尿症 Post-maturity 过度成熟 ...

例句

The management of phenylketonuria in childhood requires a multidisciplinary approach across the hospital community interface.

儿童苯丙酮尿症的管理需要多学科的协作。

Conclusion: The special bone changes in phenylketonuria were important X-ray signs suggestive of phenylketonuria .

结论：苯丙酮尿症特异性的骨骼改变是诊断苯丙酮尿症的重要X线征。

Study on brain delayed myelination and blood phenylalanine of patients with phenylketonuria.

苯丙酮尿症患儿脑髓鞘发育延迟与血苯丙氨酸浓度关系的研究。

Phenylketonuria (PKU) is one kinds of autosomal recessive disease caused by phenylalanine hydroxylase(PAH) gene mutation.

苯丙酮尿症是由于苯丙氨酸羟化酶基因突变引起的常染色体隐性遗传病。

A study of phenylketonuria heterozygotes screening in married population of Tianjin area

天津地区已婚群体苯丙酮尿症杂合子筛查

Correlation of Conventional Magnetic Resonance Imaging and Clinical Biochemistry of Brain Lesion in Children with Phenylketonuria

苯丙酮尿症儿童脑部磁共振成像与临床生化的相关性

Comparison of serum amino acid content before and after controlling pathogenetic condition in patients with phenylketonuria

苯丙酮尿症患者病情控制前后血清氨基酸含量比较

Determination of blood contents of calcium and trace elements in children with phenylketonuria on a low phenylalanine diet

饮食治疗苯丙酮尿症患儿全血钙及微量元素水平分析

Identification of novel mutations in the phenylalanine hydroxylase gene of classical phenylketonuria

经典型苯丙酮尿症苯丙氨酸羟化酶基因的新突变鉴定

Research on Fluorescence Detection System for Neonatal Phenylketonuria Screening

新生儿苯丙酮尿症荧光筛查系统的研究

Reproductive damage and its prevention for women with phenylketonuria

妇女苯丙酮尿症的生殖健康危害及其预防

The behavioral and emotional problems of patients with phenylketonuria early treated with dietotherapy

饮食治疗的苯丙酮尿症精神行为问题

Evaluation of two methods for phenylketonuria screening in newborn

新生儿苯丙酮尿症两种实验室筛查方法的质量评价

Detection of phenylketonuria heterozygotes by tandem mass spectrometry

串联质谱技术对苯丙酮尿症杂合子的检测

Determination of phenylalanine hydroxylasegene mutation of phenylketonuria in Inner Mongolia

内蒙古地区苯丙酮尿症苯丙氨酸羟化酶基因突变的检测

Advancement of Biochemical and Brain Neurological Injury in Phenylketonuria

苯丙酮尿症生化学异常与脑神经损伤关系的研究进展

Study on mental retardation and brain delayed myelination of patients with phenylketonuria

治疗延迟的苯丙酮尿症患儿脑髓鞘发育延迟与智力发育的研究

Research on Enzyme-biosensor Detecting Phenylketonuria

检验苯丙酮尿症的酶生物传感器研究

Prenatal Gene Diagnosis and Synthetic Analysis in High Risk Phenylketonuria

高危苯丙酮尿症胎儿产前基因诊断的综合分析

Analysis on the screening results of neonatal phenylketonuria in Gansu province

甘肃省新生儿苯丙酮尿症筛查结果分析