Stem cells apparently cure boy's fatal disease
The treatment uses umbilical and marrow cells to help develop normal skin. Doctors say it may move his genetic disorder 'off the incurable list' for other patients.
By Thomas H. Maugh II
Los Angeles Times Staff Writer
June 6, 2008
Using stem cells from umbilical cord blood and bone marrow, researchers have apparently cured a fatal genetic disease in a 2-year-old Minneapolis boy, a feat that could open the door for a variety of stem cell treatments.
For the first time in his life, Nate Liao is wearing normal clothes, eating food that has not been pureed and playing with his siblings.
"Nate's quality of life is forever changed," said Dr. John Wagner of the University of Minnesota Medical School, who performed the treatment. "Maybe we can take one more disorder off the incurable list."
The team has subsequently treated Nate's 5-year-old brother Jacob and is preparing to treat 9-month-old Sarah Rose Mooreland of Folsom, Calif., and hopes are high for them as well.
Nate suffers from recessive epidermolysis bullosa, a genetic disease that affects one in every 100,000 children. Such children lack a critical protein called collagen type VII that anchors the skin and lining of the gastrointestinal system to the body.
(Continued here.)
By Thomas H. Maugh II
Los Angeles Times Staff Writer
June 6, 2008
Using stem cells from umbilical cord blood and bone marrow, researchers have apparently cured a fatal genetic disease in a 2-year-old Minneapolis boy, a feat that could open the door for a variety of stem cell treatments.
For the first time in his life, Nate Liao is wearing normal clothes, eating food that has not been pureed and playing with his siblings.
"Nate's quality of life is forever changed," said Dr. John Wagner of the University of Minnesota Medical School, who performed the treatment. "Maybe we can take one more disorder off the incurable list."
The team has subsequently treated Nate's 5-year-old brother Jacob and is preparing to treat 9-month-old Sarah Rose Mooreland of Folsom, Calif., and hopes are high for them as well.
Nate suffers from recessive epidermolysis bullosa, a genetic disease that affects one in every 100,000 children. Such children lack a critical protein called collagen type VII that anchors the skin and lining of the gastrointestinal system to the body.
(Continued here.)
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