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Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 8

MONDO:0029135

Also known as: LGMD-POMGNT2 related myopathy, MDDGC8, Muscular dystrophy-dystroglycanopathy, limb-girdle, POMGNT2-related, muscular dystrophy, limb-girdle, autosomal recessive 24, muscular dystrophy-dystroglycanopathy (limb-girdle), TYPE C, 8

7 clinical trials for this condition and its sub-types.

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Broader categories

Disease (717) Nervous system disorder (243) Metabolic disease (241) Musculoskeletal system disorder (214) Hereditary disease (188) Neuromuscular disease (110) Muscular dystrophy (74) Muscle tissue disorder (56) Inborn errors of metabolism (47) Limb-girdle muscular dystrophy (17)

Trials to join now! 6 Completed 1

New study maps key tests for LGMD to speed up drug development

Knowledge-focused Completed

This study involved 116 people with Limb Girdle Muscular Dystrophy (LGMD), a group of rare muscle-weakening disorders. Researchers measured how well participants could walk, move their arms, and breathe, and asked about their daily activities and overall health. The goal was to i…

Sponsor: Virginia Commonwealth University • Aim: Knowledge-focused

Last updated Jun 27, 2026 09:09 UTC