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Polymyositis (medical condition): A muscle disease characterized by chronic muscle inflammation resulting in...more »
See also:
Dermatomyositis:
»Introduction: Dermatomyositis
»Symptoms of Dermatomyositis
»Causes of Dermatomyositis
»Tests for Dermatomyositis
»Treatments for Dermatomyositis
Polymyositis: A generalized muscle disease.
Polymyositis: myositis characterixed by weakness of limb and neck muscles and much muscle pain and swelling; progression and severity vary among individuals.
Source: WordNet 2.1
Polymyositis: progressive condition characterized by symmetric proximal muscular weakness with elevated serum levels of muscle enzymes and a skin rash, typically a purplish-red erythema on the face, and edema of the eyelids and periorbital tissue; affected muscle tissue shows degeneration of fibers with a chronic inflammatory reaction; occurs in children and adults, and in the latter may be associated with visceral cancer or other disorders of connective tissue.
Source: Diseases Database
Polymyositis: inflammation of a number of voluntary muscles simultaneously.
Source: CRISP
Polymyositis: Diseases characterized by inflammation involving multiple muscles. This may occur as an acute or chronic condition associated with medication toxicity (DRUG TOXICITY); CONNECTIVE TISSUE DISEASES; infections; malignant NEOPLASMS; and other disorders. The term polymyositis is frequently used to refer to a specific clinical entity characterized by subacute or slowly progressing symmetrical weakness primarily affecting the proximal limb and trunk muscles. The illness may occur at any age, but is most frequent in the fourth to sixth decade of life. Weakness of pharyngeal and laryngeal muscles, interstitial lung disease, and inflammation of the myocardium may also occur. Muscle biopsy reveals widespread destruction of segments of muscle fibers and an inflammatory cellular response. (Adams et al., Principles of Neurology, 6th ed, pp1404-9).
Source: MeSH 2007
These medical condition or symptom topics may be relevant to medical information for Polymyositis:
Polymyositis is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Polymyositis, or a subtype of Polymyositis,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when if affects 1 person per 2,000.
They list Polymyositis as a "rare disease".
Source - Orphanet
Polymyositis: Another name for Dermatomyositis (or close medical condition association).
»Introduction: Dermatomyositis
»Symptoms of Dermatomyositis
»Causes of Dermatomyositis
»Treatments for Dermatomyositis
Polymyositis: Polymyositis is listed as a type of (or associated with) the following medical conditions in our database:
Some of the causes of Polymyositis are included in the list below:
Read more about causes of Polymyositis (Dermatomyositis)
Some of the symptoms of Polymyositis incude:
See full list of 87 symptoms of Polymyositis (Dermatomyositis)
Treatments for Polymyositis (Dermatomyositis) include:
See full list of 10 treatments for Polymyositis
Treatment of Polymyositis: For more treatment information about Polymyositis, see treatment of Dermatomyositis (Polymyositis)
Polymyositis is an inflammatory muscle disease that causes varying degrees of decreased muscle power. (Source: excerpt from NINDS Polymyositis Information Page: NINDS)
Polymyositis is an inflammatory muscle disease that causes varying degrees of decreased muscle power. (Source: excerpt from NINDS Polymyositis Information Page: NINDS)
Dermatomyositis is one of a group of acquired muscle diseases called inflammatory myopathies. (Source: excerpt from NINDS Dermatomyositis Information Page: NINDS)
These medical disease topics may be related to Polymyositis:
Source: Diseases Database
Source - CRISP
Source - CRISP
Source - WordNet 2.1
Source: CRISP
The following list attempts to classify Polymyositis into categories where each line is subset of the next.
Source: WordNet 2.1
Source: Diseases Database
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