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  2. Dermatomyositis - Wikipedia

    en.wikipedia.org/wiki/Dermatomyositis

    Dermatomyositis (DM) is a long-term inflammatory autoimmune disorder which affects the skin and the muscles. Its symptoms are generally a skin rash and worsening muscle weakness over time. These may occur suddenly or develop over months. Other symptoms may include weight loss, fever, lung inflammation, or light sensitivity.

  3. Gottron's sign - Wikipedia

    en.wikipedia.org/wiki/Gottron's_sign

    Gottron's sign is a pathognomonic cutaneous manifestation associated with dermatomyositis (DM), which is an inflammatory disorder affecting the skin and muscles. [1] The primary lesion of dermatomyositis appears as a violaceous, macular erythema with a symmetric distribution, which may progress and become poikilodermatous (atrophic with telangiectasia and pigmentary changes) and indurated (as ...

  4. Inflammatory myopathy - Wikipedia

    en.wikipedia.org/wiki/Inflammatory_myopathy

    Around 3.2 children per million per year are diagnosed with DM (termed juvenile dermatomyositis), with an average age of onset of seven years. Diagnosis of adult DM commonly occurs between 30 and 50 years of age. PM is an adult disease, usually emerging after the age of twenty.

  5. Myositis - Wikipedia

    en.wikipedia.org/wiki/Myositis

    The three main types of idiopathic myositis (known as inflammatory myopathies) that typically test positive for autoantibodies are dermatomyositis, polymyositis, and inclusion body myositis. [4] Other autoimmune diseases, such as systemic lupus erythematosus, can also cause myositis-like symptoms. [4]

  6. List of neuromuscular disorders - Wikipedia

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

    Early adult-onset type 1; Early adult-onset type 2; Early adult-onset type 3; Myofibrillar myopathy ... Dermatomyositis; Polymyositis; Statin-associated autoimmune ...

  7. Gowers's sign - Wikipedia

    en.wikipedia.org/wiki/Gowers's_sign

    Gowers's sign is classically seen in Duchenne muscular dystrophy where it is mostly evident at 4–6 years, but also presents itself in centronuclear myopathy, myotonic dystrophy and various other conditions associated with proximal muscle weakness, including Becker muscular dystrophy, dermatomyositis and Pompe disease.

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