Scientists studying one of the world’s most serious inherited muscle diseases have found encouraging evidence that treating children much earlier—potentially before obvious symptoms develop—could make a significant difference. Researchers at Binghamton University in New York are studying the drug Vamorolone in very young boys with Duchenne muscular dystrophy (DMD), a progressive genetic disorder that causes […]
The post New Treatment Shows Remarkable Motor Improvements in Boys With Muscular Dystrophy—in Just 12 Weeks appeared first on Good News Network.
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