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The LGMD2D Foundation is working to cure alpha-sarcoglycanopathy. You can make a difference by donating today.

Have you been diagnosed with LGMD2D? Join the patient registry to be alerted of upcoming trials and to help draw attention to the disease.

Learn more about the alpha sarcoglycan gene, mRNA and protein as well as the scientific resources available for studying the protein.

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About the LGMD2D Foundation

The LGMD2D Foundation is a non-profit private foundation whose mission is to expedite the development of a cure or therapy for Limb-Girdle Muscular Dystrophy 2D (LGMD2D). In addition to educating patients and physicians, the Foundation maintains a patient registry, funds and monitors research and progress, provides financial support to accelerate clinical trials, and encourages scientific collaboration.



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by Dr. Radut