{"id":11836,"date":"2025-07-25T22:59:21","date_gmt":"2025-07-25T20:59:21","guid":{"rendered":"https:\/\/valintermed.com\/?p=11836"},"modified":"2025-07-25T22:59:21","modified_gmt":"2025-07-25T20:59:21","slug":"konechnostno-poyasnaya-myshechnaya-distrofiya-tip-1a","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/limb-lumbar-myocardial-dystrophy-type-1a\/","title":{"rendered":"Limb-girdle muscular dystrophy type 1A"},"content":{"rendered":"
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Limb-girdle muscular dystrophy type 1A (LGMD 1A) is a genetic disorder belonging to the group of myodystrophies. It is characterized by progressive muscle weakness and atrophy, primarily affecting proximal muscle groups, such as the shoulder girdle and pelvic girdle muscles. This disease is characterized by early onset and often rapid progression, which significantly worsens the quality of life of patients. Difficulties with physical activity are observed, which leads to the need for additional help and support from others. The etiopathogenesis of the disease is associated with a violation of the structure and function of muscle fibers, which is caused by mutations in the gene encoding certain proteins important for maintaining the integrity of muscle tissue.<\/p>\n

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