Symptoms of polymyositis

    • [DOC File]Symptoms of oesophageal disease - ENT Lectures

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      Respiratory/Laryngeal symptoms. Dysphagia: D. ysphagia (from the Greek dys, meaning with difficulty, and phagia, meaning to eat) arises when transport of liquid or a bolus of food along the pharyngoesophageal conduit is impaired by ... Parkinson's disease, and polymyositis. Neuromuscular disorders (eg, achalasia, diffuse esophageal spasm), many ...

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    • [DOC File]REVIEW REQUEST FOR - Anthem

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      Severe polymyositis when other treatments have been unsuccessful, intolerable, or are contraindicated (If checked, please list previous treatments and results): Primary humoral immunodeficiency (If checked, please specify): Individual has a history of recurrent sinopulmonary infections requiring antibiotic therapy

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    • [DOCX File]dptportfolios.web.unc.edu

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      Diagnosis and Treatment of Dermatomyositis in Middle-Aged Adults . Dermatomyositis, one of only three known inflammatory myopathies, is a systemic disease that mainly affects the skin and muscles in afflicted individuals but can also affect other areas of the body such as joints, the esophagus, lungs and heart.1,2 Inflammatory myopathies are generally considered to be autoimmune diseases that ...

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    • LACE index scoring tool - CAPC

      Connective tissue disease Systemic lupus erythematosus (SLE), polymyositis, mixed connective tissue disease, moderate to severe rheumatoid arthritis, and polymyalgia rheumatica AIDS AIDS-defining opportunistic infection or CD4 < 200 Moderate or severe liver or renal disease Cirrhosis with portal hypertension (e.g., ascites or variceal bleeding)

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    • [DOCX File]Specialist Working Group for Neurology - Blood

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      DM: The Biotext (2004) review included one double-blind, placebo-controlled trial considered of low quality of 15 patients with biopsy-confirmed, treatment-resistant dermatomyositis. IVIg treatment combined with prednisone led to significant improvement in muscle strength and neuromuscular symptoms of patients in the intervention group (n=8).

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    • [DOC File]Polymyositis - University of Babylon

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      Polymyositis can occur at any age, but it mostly affects adults in their 40s and 50s. It's more common in blacks than in whites, and women have it more often than men do. Polymyositis usually develops gradually over weeks or months. Periods of remission, during which symptoms improve spontaneously, rarely occur in polymyositis.

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    • [DOC File]§4 - Veterans Affairs

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      Mild: symptoms relieved by built-up shoe or arch support 0. 5277 Weak Foot, bilateral: A symptomatic condition secondary to many constitutional conditions, characterized by atrophy of the musculature, disturbed circulation, and weakness: Rate the underlying condition, minimum rating 10.

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    • [DOC File]DERMATOMYOSITIS AND POLYMYOSITIS

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      Both polymyositis and dermatomyositis have a female preponderance of 3:1. The peak age of onset is between 50 to 60; although cases have been described in all ages including children. These disorders, particularly dermatomyositis are associated with malignancy.

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    • [DOC File]Rheumatology, Chronic Fatigue Syndrome, Fibromyalgia ...

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      Chronic Fatigue Syndrome- A chronic state of sustained exhaustion that diminishes the sufferer’s physical and mental capacity. Symptoms are not fully or consistently relieved by rest. ... Signs and symptoms associated with polymyositis. Muscle weakness - proximal muscle groups of the upper and lower extremities as well as the neck.

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    • [DOCX File]Specialist Working Group for Neurology - Blood

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      [cited 7 Dec 2007]Cherin, P, Pelletier, S, Teixeira, A, et al 2002, ‘Results and long-term follow up of intravenous immunoglobulin infusions in chronic, refractory polymyositis: an open study with thirty-five adult patients’, Arthritis & Rheumatism, vol. 46, no. 2, pp. 467–74.Choy, EHS, Hoogendijk, JE, Lecky, B, …

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