phenylketonuria 中文意思是什麼
phenylketonuria
解釋
n. 名詞 【醫學】苯酮尿。adj. 形容詞 -nuric
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Research on enzyme - biosensor detecting phenylketonuria
檢驗苯丙酮尿癥的酶生物傳感器研究 -
Phenylketonuria is a condition in which phenylalanine to tyrosine conversion is diminished because the enzyme phenylalanine hydroxylaze is deficient.
苯丙酮酸尿癥是一種由於苯丙氨酸羥化酶缺乏，苯丙氨酸轉變成酪氨酸的過程被削弱的病。 -
Analysis on neonatal screening for phenylketonuria in fujian, china
福建省新生兒苯丙酮尿癥篩查狀況分析 -
Comparative study on secondary seizure to tetrahydrobiopterin and phenylketonuria
高苯丙氨酸血癥的抽搐機制研究 -
Study on incidence and type of phenylketonuria and congenital hypothyroidism in newborn in tangshan city
唐山市新生兒苯丙酮尿癥與先天性甲狀腺功能減低癥發病現狀分析與研究 -
For premature infants and babies with metabolic disorders such as phenylketonuria more specialized formulas can be recommended by a pediatrician or specialist nurse
對于出現代謝紊亂如苯丙酮酸尿癥的早產兒，則需要由兒科醫生或專業護士推薦出更特殊的配方奶。 -
Phenylketonuria ( pku ) is an inherited metabolic disease that results in mental retardation and other neurological problems when treatment is not started within the first few weeks of life. the disease arises from the deficiency of a single enzyme, phenylalanine hydroxylase, which converts the essential amino acid, phenylalanine, to another amino acid, tyrosine. failure of the conversion to take place results in a buildup of phenylalanine in the body that then damages the central nervous system
苯丙酮尿癥（ pku ）是一種智力發育不全的先天性疾病，患者由於肝贓內苯丙氨酸羥化酶缺乏，苯丙氨酸不能正常代謝為酪氨酸，從而導致苯丙氨酸在肌體組織內積累，引起腦損傷和累進性精神障礙，臨床表現為智力低下，頭發顏色轉黃，尿有異臭味，重者似鼠臭。
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