Live Blogger: Lauren Heinzinger
Editors: Ryan Schildcrout, Brenna Saladin
This piece was written live during the 10th annual RNA Symposium, “RNA Frontiers: From Mechanisms to Medicine” hosted by the University of Michigan’s Center for RNA Biomedicine.
Huntington’s Disease (HD) is a fatal hereditary neurodegenerative disorder that typically emerges between the ages of 30 and 50. It’s a progressive disease that damages neurons in the brain that control voluntary body movement, resulting in uncontrolled dance-like movements called chorea and abnormal postures. Other symptoms of HD include changes in behavior, emotion, personality, and thinking. Despite modern medicine and all of our amazing medical advancements, there is still no cure for HD. This makes it especially important to understand the mechanisms underlying how HD damages these important neural cells.
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