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  2. Limb–girdle muscular dystrophy - Wikipedia

    en.wikipedia.org/wiki/Limbgirdle_muscular...

    The diagnosis of limbgirdle muscular dystrophy can be done via muscle biopsy, which will show the presence of muscular dystrophy, and genetic testing is used to determine which type of muscular dystrophy a patient has. Immunohistochemical dystrophin tests can indicate a decrease in dystrophin detected in sarcoglycanopathies.

  3. 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.

  4. Muscular dystrophy - Wikipedia

    en.wikipedia.org/wiki/Muscular_Dystrophy

    The diagnosis of muscular dystrophy is based on the results of muscle biopsy, ... Limbgirdle muscular dystrophy: Multiple Multiple AD, AR: Any Upper arms and legs

  5. LAMA2 related congenital muscular dystrophy - Wikipedia

    en.wikipedia.org/wiki/LAMA2_related_congenital...

    LAMA2 muscular dystrophy; Other names: Congenital muscular dystrophy type 1A (MDC1A) or Merosin-deficient congenital muscular dystrophy, Late-onset LAMA2 muscular dystrophy or limb girdle muscular dystrophy 23 (LGMDR23), Laminin subunit alpha-2 muscular dystrophy. Diagrammatic illustration of laminin-211 or Laminin-alpha2 chain.

  6. List of neuromuscular disorders - Wikipedia

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

    Limb girdle muscular dystrophies (LGMD) as defined by the European Neuromuscular Centre in 2018. [1] [2] They are named by the following system: LGMD, recessive or dominant inheritance (R or D), order of discovery (number), affected protein.

  7. 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 ...

  8. Woman with Muscular Dystrophy Signed Up for Dating App ... - AOL

    www.aol.com/lifestyle/woman-muscular-dystrophy...

    Diagnosed with a form of Limb-girdle muscular dystrophy when she was 2 years old, Fegley says she could walk up until she was in the 10th grade, but began using a wheelchair after undergoing ...

  9. Glycogen storage disease type II - Wikipedia

    en.wikipedia.org/wiki/Glycogen_storage_disease...

    Glycogen storage disease type II (GSD-II), also called Pompe disease, and formerly known as GSD-IIa or Limbgirdle muscular dystrophy 2V, is an autosomal recessive metabolic disorder [1] which damages muscle and nerve cells throughout the body.

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