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单词 Tay-Sachs disease
释义 Tay-Sachs disease【医】 家族黑蒙性白痴 Tay-Sachs disease  Tay-Sachs disease  AHD:  [t³“s²ks”] D.J.  [6te!7s#ks]K.K.  [6te7s#ks]n.(名词)A hereditary disease that affects young children almost exclusively of eastern European Jewish descent, in which an enzyme deficiency leads to the accumulation of gangliosides in the brain and nerve tissue, resulting in mental retardation, convulsions, blindness, and, ultimately, death.泰氏-萨氏病:一种几乎专门传染东欧犹太人后裔幼童的遗传性疾病,在病中由于缺乏酶导致大脑和神经组织中神经节甙脂的增多,造成思想迟钝、痉挛、失明,并且最终导致死亡语源:After Warren Tay  (1843-1927), British physician, and Bernard Sachs  (1858-1944), American neurologist 源自沃伦 泰 (1843-1927年),英国医生,和 萨克斯 (1858-1944年),美国神经科专门医师
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