Dermatomyositis
Dermatomyositis: Introduction
Dermatomyositis:
Polymyositis
is an inflammatory muscle disease that causes varying degrees of decreased
muscle power.
(Source: excerpt from NINDS Polymyositis Information Page: NINDS)
... more about Dermatomyositis.
Dermatomyositis: A muscle disease characterized by chronic muscle inflammation resulting in progressive muscle weakness and a characteristic rash.
More detailed information about the symptoms,
causes, and treatments of Dermatomyositis is available below.
Symptoms of Dermatomyositis
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symptoms of Dermatomyositis
Dermatomyositis: Complications
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Disease Topics Related To Dermatomyositis
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Medical Textbooks Online about Dermatomyositis
Book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.
Less Common Symptoms of Dermatomyositis
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Diagnostic Tests for Dermatomyositis
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Wrongly Diagnosed with Dermatomyositis?
Dermatomyositis: Marketplace Products, Discounts & Offers
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Misdiagnosis and Dermatomyositis
Psoriasis often undiagnosed cause of skin symptoms in children: Children who suffer
from the skin disorder called psoriasis can often go undiagnosed.
The main problem is that psoriasis is rare...read more »
Dermatomyositis in breast cancer: Dermatomyositis is a serious connective-tissue disease related to polymyositis
that is characterized by inflammation of the muscles and the skin. The cause is
unknown, but it may result from...read more »
Read more about Misdiagnosis and Dermatomyositis
Dermatomyositis: Research Doctors & Specialists
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Causes of Dermatomyositis
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Treatments for Dermatomyositis
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treatments for Dermatomyositis
Videos for Dermatomyositis
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Patient Surveys for Dermatomyositis
Prognosis for Dermatomyositis
Prognosis for Dermatomyositis:
20% die in first year in extreme cases, 5-16 years survival in children is 75%, 2 to several years survival in chronic forms, cancer removal may cure the condition
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Reseach about Dermatomyositis
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Clinical Trials for Dermatomyositis
The US based website ClinicalTrials.gov lists information on both federally
and privately supported clinical trials using human volunteers.
Some of the clinical trials listed on ClinicalTrials.gov for Dermatomyositis include:
See full list of 42
Clinical Trials for Dermatomyositis
Statistics for Dermatomyositis
Dermatomyositis: Broader Related Topics
Types of Dermatomyositis
Stories from Users Related to Dermatomyositis
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Article Excerpts about Dermatomyositis
NINDS Polymyositis Information Page: NINDS (Excerpt)
Polymyositis
is an inflammatory muscle disease that causes varying degrees of decreased
muscle power.
(Source: excerpt from NINDS Polymyositis Information Page: NINDS)
NINDS Dermatomyositis Information Page: NINDS (Excerpt)
Dermatomyositis is one of a group of acquired
muscle diseases called inflammatory myopathies.
(Source: excerpt from NINDS Dermatomyositis Information Page: NINDS)
Definitions of Dermatomyositis:
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)
Myositis characterized by weakness of limb and neck muscles and much muscle pain and selling accompanied by skin rash affecting cheeks and eyelids and neck and chest and limbs; progression and severity vary among individuals
- (Source - WordNet 2.1)
Dermatomyositis is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Dermatomyositis, or a subtype of Dermatomyositis,
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 it affects 1 person per 2,000.
They list Dermatomyositis as a "rare disease".
Source - Orphanet
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