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  2. Inclusion body myositis - Wikipedia

    en.wikipedia.org/wiki/Inclusion_body_myositis

    Inclusion body myositis (IBM) (/ m aɪ oʊ ˈ s aɪ t ɪ s /) (sometimes called sporadic inclusion body myositis, sIBM) is the most common inflammatory muscle disease in older adults. [2] The disease is characterized by slowly progressive weakness and wasting of both proximal muscles (located on or close to the torso ) and distal muscles (close ...

  3. Fibrodysplasia ossificans progressiva - Wikipedia

    en.wikipedia.org/wiki/Fibrodysplasia_ossificans...

    Fibrodysplasia ossificans progressiva (/ ˌ f aɪ b r oʊ d ɪ ˈ s p l eɪ ʒ (i) ə ɒ ˈ s ɪ f ɪ k æ n z p r ə ˈ ɡ r ɛ s ɪ v ə /; [1] abbr. FOP), also called Münchmeyer disease or formerly myositis ossificans progressiva, is an extremely rare connective tissue disease in which fibrous connective tissue such as muscle, tendons, and ligaments turn into bone tissue (ossification).

  4. Polymyositis - Wikipedia

    en.wikipedia.org/wiki/Polymyositis

    Polymyositis and the associated inflammatory myopathies have an associated increased risk of cancer. [3] The features they found associated with an increased risk of cancer were older age, age greater than 45, male sex, difficulty swallowing, death of skin cells, cutaneous vasculitis, rapid onset of myositis (<4 weeks), elevated creatine kinase, higher erythrocyte sedimentation rate and higher ...

  5. Inflammatory myopathy - Wikipedia

    en.wikipedia.org/wiki/Inflammatory_myopathy

    It can also be associated with underlying cancer. The main classes of idiopathic inflammatory myopathy are polymyositis (PM), dermatomyositis (DM) (including juvenile, amyopathic, and sine-dermatitis form), inclusion-body myositis (IBM), immune-mediated necrotising myopathy (IMNM), and focal autoimmune myositis. [1]

  6. Scleromyositis - Wikipedia

    en.wikipedia.org/wiki/Scleromyositis

    Scleromyositis, is an autoimmune disease (a disease in which the immune system attacks the body). People with scleromyositis have symptoms of both systemic scleroderma and either polymyositis or dermatomyositis, and is therefore considered an overlap syndrome.

  7. Scleroderma - Wikipedia

    en.wikipedia.org/wiki/Scleroderma

    Mixed connective tissue disease, systemic lupus erythematosus, polymyositis, dermatomyositis [1] Treatment: Supportive care [1] Medication: Corticosteroids, methotrexate, non-steroidal anti-inflammatory drugs (NSAIDs) [2] Prognosis: Localized: Normal life expectancy [7] Systemic: Decreased life expectancy [3] Frequency: 3 per 100,000 per year ...

  8. Life expectancy isn't rising as much, the health consequences ...

    www.aol.com/lifestyle/life-expectancy-isnt...

    Life expectancy may be plateauing. Don’t expect your grandkids to live to 200 years old. A study published on Monday suggests we may be reaching our limit in terms of life expectancy and that ...

  9. Antisynthetase syndrome - Wikipedia

    en.wikipedia.org/wiki/Antisynthetase_syndrome

    Those with anti-Jo1 antibodies had less remission of myositis and more relapses than those with anti-PL-12 and anti-PL-7 antibodies. [64] Anti-Jo-1 and anti-Ro52 antibodies co-occurring were linked to an increased risk of neoplasm, a symptomatic severe variant of interstitial lung disease, myositis, and arthritis exacerbation. [20]