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LGMD2D Foundation
  • Home
  • About Us
  • Patient Resources
  • Trials & Research
  • Donate
  • Contact Us

Raising awareness to cure LGMD2D.

Raising awareness to cure LGMD2D.Raising awareness to cure LGMD2D.Raising awareness to cure LGMD2D.

Raising awareness to cure LGMD2D.

Raising awareness to cure LGMD2D.Raising awareness to cure LGMD2D.Raising awareness to cure LGMD2D.

Our Mission

Patient Registry

What is LGMD2D?

To support research and clinical trials to speed the development of treatments and a cure for LGMD2D.

About us

What is LGMD2D?

Patient Registry

What is LGMD2D?

Limb-Girdle Muscular Dystrophy, type 2D / R3 (LGMD2D), is caused by mutations in the alpha-sarcoglyan gene that lead to a deficiency of functional alpha-sarcoglycan protein. 

LGMD2D causes weakness of muscles in the hip, shoulder, and abdomen. 

Learn more

Patient Registry

Patient Registry

Patient Registry

The International LGMD2D Patient Registry is free to join and is currently the only database for all patients afflicted with LGMD2D. 

Register Now

Help us find a cure.

Your generous donation will help support research to find effective treatments or a cure for LGMD2D.

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LGMD Community Partners

The Speak Foundation
LGMD Awareness Foundation
Jain Foundation
LGMD2I Fund
  • LGMD2I Fund
  • The Speak Foundation
  • LGMD Awareness Foundation
  • Jain Foundation
  • LGMD2I Fund
  • The Speak Foundation
  • LGMD Awareness Foundation

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LGMD2D Foundation

Copyright © 2023 LGMD2D Foundation - All Rights Reserved. LGMD2D Foundation is a 501(c)(3), Est. 2013.

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