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  2. Calpainopathy - Wikipedia

    en.wikipedia.org/wiki/Calpainopathy

    Calpainopathy is the most common type of autosomal recessive limb-girdle muscular dystrophy (LGMD). [2] It preferentially affects the muscles of the hip girdle and shoulder girdle. No disease modifying pharmaceuticals have been developed as of 2019, although physical therapy, lifestyle modification, and orthopedic surgery can address symptoms.

  3. Limb–girdle muscular dystrophy - Wikipedia

    en.wikipedia.org/wiki/Limb–girdle_muscular...

    Limb–girdle muscular dystrophy (LGMD) is a genetically heterogeneous group of rare muscular dystrophies that share a set of clinical characteristics. [7] It is characterised by progressive muscle wasting which affects predominantly hip and shoulder muscles. [ 8 ]

  4. List of neuromuscular disorders - Wikipedia

    en.wikipedia.org/wiki/List_of_neuromuscular...

    Distal muscular dystrophy, also called distal myopathy, is essentially any muscle disease that preferentially affects the hands and/or feet, a much less common pattern than proximal muscle weakness. Late adult-onset type 1; Late adult-onset type 2a; Late adult-onset type 2b; Early adult-onset type 1; Early adult-onset type 2; Early adult-onset ...

  5. Muscular dystrophy - Wikipedia

    en.wikipedia.org/wiki/Muscular_Dystrophy

    Distal limb muscles, limb-girdle, heart Symptoms include muscle weakness and wasting, starting in the distal limb muscles and progressing to involve the limb–girdle muscles. Most patients also have cardiac conduction defects and arrhythmias. [18] [19] Facioscapulohumeral muscular dystrophy: 158900: DUX4: AD: Adolescence

  6. Bethlem myopathy - Wikipedia

    en.wikipedia.org/wiki/Bethlem_myopathy

    The symptoms of Bethlem myopathy may overlap with other conditions including Emery–Dreifuss muscular dystrophy, congenital muscular dystrophies, limb girdle muscular dystrophies, FHL1-related myopathies (X-linked myopathy with postural muscle atrophy, reducing body myopathy, and scapuloperoneal myopathy), and some forms of Ehlers–Danlos ...

  7. Inclusion body myositis - Wikipedia

    en.wikipedia.org/wiki/Inclusion_body_myositis

    Muscular dystrophy (e.g., limb girdle muscular dystrophy) must be considered as well. [citation needed] sIBM can be mistaken for physical deconditioning. [1] Hereditary myopathies can mimic sIBM, both in signs and symptoms and in the appearance of muscle biopsies.

  8. Mom Has 3 Days to Get Son Life-Saving Treatment for Muscular ...

    www.aol.com/mom-3-days-son-life-150759249.html

    “CK stands for creatine kinase, an enzyme that leaks out of damaged muscle,” the Muscular Dystrophy Association explains. “When elevated CK levels are found in a blood sample, it usually ...

  9. Polymyalgia rheumatica - Wikipedia

    en.wikipedia.org/wiki/Polymyalgia_rheumatica

    Pain can also occur in the groin area and in the buttocks. The pain can be limited to one of these areas as well. It is a disease of the "girdles" meaning shoulder girdle or pelvic girdle. Fatigue and lack of appetite (possibly leading to weight loss) Anemia; An overall feeling of illness or flu-like symptoms.

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