Svitlana Garbuzova-Davis,Paul R. Sanberg,Sylvia Gografe
申请号：
US12168608
公开号：
US09173907B2
申请日:
2008.07.07
申请国别(地区):
US
年份:
2015
代理人:
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 Sanfilippos syndrome, Hunters syndrome, Hurlers syndrome, Tay-Sachs disease, Gauchers disease, von Gierkes disease, Pompes disease, Cori disease, Andersen disease, McArdles disease, Hers disease, Tauris disease or Type IX glycogen storage disease.
