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Miyoshi myopathy

MONDO:0009685

A distal myopathy, characterized by weakness in the distal lower extremity posterior compartment (gastrocnemius and soleus muscles) and associated with difficulties in standing on tip toes.

Also known as: MM, Miyoshi distal myopathy, Miyoshi muscular dystrophy, MMD1, Miyoshi muscular dystrophy 1, Miyoshi muscular dystrophy type 1, muscular dystrophy, distal, late onset, autosomal recessive

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

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Sub-types

Miyoshi muscular dystrophy 3 (1) Miyoshi muscular dystrophy 1 (0) Miyoshi muscular dystrophy 2 (0)

Broader categories

Disease (717) Nervous system disorder (243) Musculoskeletal system disorder (214) Hereditary disease (188) Neuromuscular disease (110) Muscular dystrophy (74) Muscle tissue disorder (56) Human disease (15) Myopathy (14) Skeletal muscle disorder (10)
Trials to join now! 5 Not yet finished but already full! 1
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  • Can MRI scans reveal the hidden pattern of muscle damage in a rare muscular dystrophy?

    Knowledge-focused Ongoing

    This study aims to describe the pattern of muscle involvement in people with limb girdle muscular dystrophy caused by mutations in the anoctamin 5 gene. Researchers will collect and analyze MRI scans from 200 participants to see which muscles are affected and how much fat replace…

    Sponsor: Rigshospitalet, Denmark • Aim: Knowledge-focused

    Last updated Aug 14, 2026 00:00 UTC

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