摘要:
A method of treating a fetus or embryo suspected of having a congenital condition that involves an abnormal or missing protein, the method has the steps of a. providing a plurality of human umbilical cord blood in a form suitable for intravenous administration; a b. administering the human umbilical cord blood cells to a mother carrying a fetus of embryo suspected of having said congenital condition. Such congenital conditions include Sanfilippo's syndrome, Hunter's syndrome, Hurler's syndrome, Tay-Sachs disease, Gaucher's disease, von Gierke's disease, Pompes disease, Cori disease, Andersen disease, McArdle's disease, Hers disease, Tauri's disease or Type IX glycogen storage disease.
摘要翻译:一种治疗怀疑患有涉及异常或缺失蛋白质的先天性病症的胎儿或胚胎的方法,具有以下步骤:a。 提供适合于静脉内施用形式的多种人脐带血; a b。 对携带怀疑有先天性胚胎的胎儿的母亲施用人脐带血细胞。 这种先天性病症包括Sanfilippo综合征,亨特综合征,赫勒勒综合征,泰萨克病,戈谢病,冯·吉尔克病,庞培病,康利病,安徒生病,麦卡德尔病,赫斯病,牛磺病或1型糖原贮积病。
摘要:
A method of treating a fetus or embryo suspected of having a congenital condition that involves an abnormal or missing protein, the method has the steps of a. providing a plurality of human umbilical cord blood in a form suitable for intravenous administration; a b. administering the human umbilical cord blood cells to a mother carrying a fetus of embryo suspected of having said congenital condition. Such congenital conditions include Sanfilippo's syndrome, Hunter's syndrome, Hurler's syndrome, Tay-Sachs disease, Gaucher's disease, von Gierke's disease, Pompes disease, Cori disease, Andersen disease, McArdle's disease, Hers disease, Tauri's disease or Type IX glycogen storage disease.
摘要翻译:一种治疗怀疑患有涉及异常或缺失蛋白质的先天性病症的胎儿或胚胎的方法,具有以下步骤:a。 提供适合于静脉内施用形式的多种人脐带血; a b。 对携带怀疑有先天性胚胎的胎儿的母亲施用人脐带血细胞。 这种先天性病症包括Sanfilippo综合征,亨特综合征,赫勒勒综合征,泰萨克病,戈谢病,冯·吉尔克病,庞培病,康利病,安徒生病,麦卡德尔病,赫斯病,牛磺病或1型糖原贮积病。