303 top medical experts on Amyopathic dermatomyositis across 38 countries and 26 U.S. states, including 169 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Amyopathic dermatomyositis: Amyopathic dermatomyositis is a form of dermatomyositis characterized by the presence of typical skin findings without muscle weakness.Some of the skin changes that suggest dermatomyositis include a pink rash on the face, neck, forearms and upper chest; Gottron's papules and heliotrope eyelids .Pruritis and photosensitivity are common, as is scalp inflammation and thinning of the hair.While patients with amyopathic dermatomyositis should not have clinically evident muscle weakness, minor muscle abnormalities may be included. Fatigue is reported in at least 50% of patients.Some cases have been associated with internal malignancy and/or interstitial lung disease.Treatment may include sun avoidance, ample use of sunscreen, topical corticosteroids , antimalarial agents, methotrexate , mycophenolate mofetil , or intravenous (IV) immunoglobulin .
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
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