27 Jan FSHD NEWS: How CRISPR could lead to a cure for muscular dystrophy
Posted at 23:14h in Uncategorized
Your donations have played a part in this important discovery for a potential treatment and cure for FSHD. The Chris Carrino Foundation for FSHD is acknowledged in the official paper for this research. Your continued support is crucial to advance these findings. Thanks to Dr. Jones and his team for their dedication.
The promise of new CRISPR gene-editing technology has always been that it might lead to a cure for specific genetic diseases. Recently published findingsfrom a team of researchers at the University of Massachusetts Medical School in Worcester, Mass., suggest that a modified form of this CRISPR gene-editing technology may eventually result in a cure for facioscapulohumeral muscular dystrophy (FSHD), a form of the disease that leads to progressive muscular degeneration in the face, shoulder blades and upper arms.