智力发育不全的的英文

• oligophrenic

• "智力"英文翻译    intelligence; mentality; hab ...
• "发育不全"英文翻译    hypoplasia; atelia; ateliosi ...
• "的"英文翻译    4次方是 The fourth power of 2 i ...
• "智力发育不全" 英文翻译 :    intellectual deficiency; intellectual maldevelopment; oligophrenia
• "小眼智力发育不全" 英文翻译 :    oligophrenia microphthalmus
• "发育不全的" 英文翻译 :    abortive; agennetic; aplastic; ateliotic; depauperate; hypogenetic; hypoplastic; immature; semideveloped; uadergtown; under developed; under development; undergrown; vestigial
• "苯丙酮尿性智力发育不全" 英文翻译 :    phenylpyruvic oligophrenia
• "智力发育不全, 精神幼稚病" 英文翻译 :    oligophrenia
• "智力发育不全-小眼球综合征" 英文翻译 :    whitnall-norman syndrome
• "智力发育不全性苯丙酮尿" 英文翻译 :    imbecillitas phenylpyruvica
• "悖德狂,悖德性智力发育不全" 英文翻译 :    moral oligophrenia
• "精神发育不全 精神幼稚症 智力发育不全" 英文翻译 :    oligophrenia
• "头发育不全的" 英文翻译 :    atelocephalous
• "苯丙酮酸尿性智力发育不全" 英文翻译 :    imbecillitas phenylpyruvica
• "苯丙酮酸尿性智力发育不全,苯酮尿症" 英文翻译 :    imbecilitas phenylpyruvica
• "皮肤松弛-角膜混浊-智力发育不全综合征" 英文翻译 :    cutis laxa-corneal clouding-oligophrenia syndrome
• "遗传性智力发育不全-小脑脊髓变性" 英文翻译 :    hereditary digophrenia cerebellospinal cord degeneration
• "遗传性智力发育不全-小脑脊髓变性综合征" 英文翻译 :    hereditary oligophrenia-cerebellospinal cord degeneration syndrome
• "遗传性智力发育不全-小脑晶体变性综合征" 英文翻译 :    hereditary digophrenia cerebellolental syndrome
• "智力发育不全-釉质形成缺陷-多汗综合征" 英文翻译 :    brunauer syndrome
• "智力发育不全性苯丙酮尿症" 英文翻译 :    oligophrenia phenyl pyruvic aciduria; oligophrenia phenylpyruvica; oligophrenia phenyylpyruvica
• "智力发育不健全" 英文翻译 :    incomplete development of mind
• "发育不全的地区" 英文翻译 :    immature region
• "发育不全的火山" 英文翻译 :    abortive volcano
• "发育不全的模式" 英文翻译 :    immature pattern

• 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
  苯丙酮尿症（ pku ）是一种智力发育不全的先天性疾病，患者由于肝赃内苯丙氨酸羟化酶缺乏，苯丙氨酸不能正常代谢为酪氨酸，从而导致苯丙氨酸在肌体组织内积累，引起脑损伤和累进性精神障碍，临床表现为智力低下,头发颜色转黄，尿有异臭味，重者似鼠臭。