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  2. 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 ...

  3. Sporadic late-onset nemaline myopathy - Wikipedia

    en.wikipedia.org/wiki/Sporadic_late-onset...

    Sporadic late-onset nemaline myopathy, or SLONM, is a very rare disease, one of the nemaline myopathies, causing loss of muscle bulk and weakness in the legs but sparing the cranial nerves, and beginning its clinical course after age 40. [1]

  4. Camptocormia - Wikipedia

    en.wikipedia.org/wiki/Camptocormia

    Idiopathic primary BSS is a late-onset myopathy with progressive muscular weakness that is detected on the spinal extensor muscles in elderly patients and is more predominant in females. [2] The pathogenesis of primary BSS is typically related to fibrosis and fatty infiltration of muscular tissues and to mitochondrial changes due to the aging ...

  5. LAMA2 related congenital muscular dystrophy - Wikipedia

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

    The second type is the late onset LAMA2 muscular dystrophy or late onset LAMA2-MD. The age of presentation of late onset LAMA2-MD ranges from early childhood to adulthood. It usually has a mild clinical presentation in the form of progressive spine and joint contractures, and cardiac and respiratory failure. [1]

  6. Statin-associated autoimmune myopathy - Wikipedia

    en.wikipedia.org/wiki/Statin-associated...

    Statin-associated autoimmune myopathy (SAAM), also known as anti-HMGCR myopathy, is a very rare form of muscle damage caused by the immune system in people who take statin medications. [1] However, there are cases of SAAM in patients who have not taken statin medication, and this can be explained by the exposure to natural sources of statin ...

  7. Zaspopathy - Wikipedia

    en.wikipedia.org/wiki/Zaspopathy

    Late-onset distal myopathy, Markesbery-Griggs type Zaspopathy has an autosomal dominant pattern of inheritance . Zaspopathy , [ 1 ] also called ZASP-related myofibril myopathy , [ 2 ] is a novel autosomal dominant [ 3 ] form of progressive muscular dystrophy , first described in 2005.

  8. Acquired non-inflammatory myopathy - Wikipedia

    en.wikipedia.org/wiki/Acquired_non-inflammatory...

    Symptoms are usually weakness of the proximal muscles, neck flexor, and in extreme cases, respiratory muscle weakness can also occur. [1] Corticosteroids have not only been found to cause some degree of muscle atrophy, but also a local or diffuse cell death. These side effects are more common in women than in men, for reasons that are unknown. [6]

  9. Myopathy - Wikipedia

    en.wikipedia.org/wiki/Myopathy

    In medicine, myopathy is a disease of the muscle [1] in which the muscle fibers do not function properly. Myopathy means muscle disease ( Greek : myo- muscle + patheia -pathy : suffering ). This meaning implies that the primary defect is within the muscle, as opposed to the nerves (" neuropathies " or " neurogenic " disorders) or elsewhere (e.g ...