LAMA2-related muscular dystrophy
MONDO:0100228Any muscular dystrophy in which the cause of the disease is a mutation in the LAMA2 gene.
Also known as: LAMA2-related muscular dystrophy
8 clinical trials for this condition and its sub-types, 2 tagged with LAMA2-related muscular dystrophy itself.
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Sub-types of LAMA2-related muscular dystrophy
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New study tracks toddlers with rare muscle disease to prep for future treatments
Knowledge-focused Recruiting nowThis study watches how children under 5 with LAMA2-related muscular dystrophy move and develop over two years. Researchers will test muscle function, swallowing, breathing, and collect blood samples. The goal is to learn more about the disease so future treatments can be tested e…
Sponsor: Nationwide Children's Hospital • Aim: Knowledge-focused
Last updated Aug 21, 2026 00:00 UTC
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A protein clue in the fight against muscular dystrophy?
Knowledge-focused Recruiting nowThis study looks at whether levels of a protein called HMGB1 are different in people with LAMA2-related muscular dystrophy, a condition that causes severe muscle weakness. Researchers will measure HMGB1 in blood and muscle samples already collected from about 25 patients. The goa…
Sponsor: IRCCS San Raffaele • Aim: Knowledge-focused
Last updated Aug 06, 2026 00:00 UTC