英语释义

• 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

片语

Classical phenylketonuria典型的苯丙酮酸尿

phenylketonuria trustworthy苯丙酮尿癥

Malignancy phenylketonuria恶性苯丙酮尿癥

maternal phenylketonuria母体苯丙酮尿癥

congenital phenylketonuria先天性苯酮尿癥

atypical phenylketonuria非典型苯丙酮酸尿

phenylketonuria PKU苯丙酮尿癥

classic phenylketonuria典型性苯丙酮酸尿

phenylketonuria screening苯丙酮尿癥筛查

英汉例句

• objective to make a further understanding of mri manifestations of the brain in maternal phenylketonuria (mpku) offspring.

  目的提高对母亲苯丙酮尿癥（mpku）后代脑mri表现的认识。

• the comparison of abr changes at the beginning of therapy against congenital hypothyroidism and phenylketonuria and later could serve as an objective criteria for follow-up of therapeutic efficiency.

  先天性甲状腺功能低下及苯丙酮尿癥的治疗早晚的abr对比观察，可作为疗效随访和追蹤观察的客观指标。

• this method is suited for identifying errors of amino acid metabolism and phenylketonuria in particular.

  是筛查氨基酸代谢病尤其筛查苯丙酮尿癥的準确而简便的方法。

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

  儿童苯丙酮尿癥的管理需要多学科的协作。

• borsi batki suffers from phenylketonuria (pku), a metabolic disorder that if undetected, can lead to problems with brain development, progressive mental retardation, brain damage and seizures.

  她患有苯丙酮酸尿癥，这是一种先天性代谢异常病，会影响大脑发育、损伤脑部神经和损害智力。

• the eeg in 94 patients with phenylketonuria was analyzed. the abnormality rate of eeg was 65%, mainly showing epileptiform discharges(80%), partly showing background activity abnormality(20%).

  本文分析94例苯丙酮尿癥患者的脑电图，结果异常率为65％，异常表现以痫样放电为主80％，少数为背景活动异常（20％）。

• objective to establish a simple, accurate and rapid method for screening of the mutant genes in phenylketonuria (pku).

  目的建立一种简便、準确和快速的筛查苯丙酮尿癥（pku）突变基因的方法。

• urine sample of the normal children and children patients with phenylketonuria or neuroblastoma were analysed by two methods.

  并对正常儿、苯丙酮尿癥患儿、神经母细胞瘤患儿的尿标本进行了两种方法的对比研究。

• as phenylalanine dehydrogenase is used to determine the concentration of plasma phenylalanine for monitoring of phenylketonuria and synthesize l-amino acids, it is drawing more and more attention.

  苯丙氨酸脱氢酶因在临床上可用作苯丙酮尿癥的检测用酶，工业上可用于合成手性氨基酸而越来越受到关注。

• objective: to explore effective dietary regimens in treating phenylketonuria (pku) after summing up 20 years practice in 652 patients.

  目的总结20年对652例苯丙酮尿癥患儿进行低苯丙氨酸饮食治疗经验，探讨有效的饮食控制方案。