For years, muscular dystrophy (MD) has presented a daunting challenge to patients and families worldwide. However, recent developments in research offer a sign of hope for the future. Scientists are tirelessly working on groundbreaking treatments that aim to not only manage symptoms but also to reverse the progression of this debilitating disease.
In 1993, collaborative efforts from the laboratories of Drs. Harry T. Orr and Huda Y. Zoghbi found out that SCA1 is because of the enlargement of the CAG repeat somewhere inside a affected person’s DNA. CAG repeats trigger a polyglutamine enlargement within the protein which the mutated gene encodes; In such cases, the team later on determined th
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