酮尿
tónɡ niào
- ketonuria
酮尿-
通过在智能发育异常儿童中筛查特殊的一类遗传性代谢病&苯内酮尿症（phenylketonuria，PKU），以了解PKU在儿童精神发育迟滞中的病因学意义。
To know its etiological significance in MR by screening a kind of particular inheritance metabolism disease called Phenylketonuria ( PKU ) in children with MR.
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苯酮尿症的分子研究及其基因型表型相关性的研究进展
Progress of Molecular Study and Correlation Analysis between Genotypes and Phenotypes in Phenylketonuria
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临床主要表现为低血糖、酮血、酮尿、离群、厌食、运动失调、麻木、最后死亡。
The clinical signs are hypoglycemia , ketonemia , ketonuria , disperse , anorexia , ataxia , anaesthesia and final death . To lucubrate the Pregnancy Toxemia of sheep .