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Her muscles and ligaments are turning to bone When she was 9 or 10 months old, Enjoyed reading this she started to develop other small masses on her skull and along her spine. They went back to the pediatrician, who ventured several guesses, but Floyd seemed fine otherwise, so they moved on. Find A Product That Goes Deep Into The Pores, Provides Light Exfoliation And Conditioning, And Does Not Leave Any Residue. | Net Lucy WhiteLiving in shadows: A child’s rare disorder “One single genetic letter out of 6 billion,” Kaplan said; 97% of FOP patients have it. By identifying the gene, scientists were able to find the protein the gene encoded: an enzyme that basically causes a reaction that forms bone. Usually, the enzyme works only when it’s turned on, to fix broken bones, but in FOP patients, that on/off switch is on all the time. “The bone that forms is perfectly normal bone,” Kaplan article source said. “It’s just too much of a good thing.” His team and others are now looking to develop drugs that block the “on” switch. Research in rare diseases cheers is often limited. Kaplan first became interested in FOP when he saw two FOP patients in 1985. He saw how the disease robbed kids of their childhood; it most often starts presenting symptoms before the age of 5.

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