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Other Names for this Disease
- Juvenile myositis
- Juvenile polymyositis
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adult dermatomyositis and polymyositis. It typically affects children ages 2 to 15 years, with symptoms that include weakness of the muscles close to the trunk of the body, inflammation, edema, muscle pain, fatigue, skin rashes, abdominal pain, fever, and contractures. Children with juvenile dermatomyositis may have difficulty swallowing and breathing, and the heart may also be affected. About 20 to 30 percent of children with juvenile dermatomyositis develop calcium deposits in the soft tissue. Affected children may not show higher than normal levels of the muscle enzyme creatine kinase in their blood but have higher than normal levels of other muscle enzymes.Juvenile dermatomyositis has some similarities to
Last updated: 5/31/2011
- Inflammatory Myopathies Fact Sheet. National Institute of Neurological Disorders and Stroke (NINDS). February 2011; http://www.ninds.nih.gov/disorders/inflammatory_myopathies/detail_inflammatory_myopathies.htm. Accessed 5/31/2011.
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- MedlinePlus, the National Library of Medicine Web site designed to help you research your health questions, provides general information on myositis. Click on the link to view this information.
- The National Institute of Neurological Disorders and Stroke (NINDS) collects and disseminates research information related to neurological disorders. Click on the link to view information on this topic.
- The Myositis Association provides basic information on juvenile myositis.
In Depth Information
- The Online Mendelian Inheritance in Man (OMIM) database contains genetics resources that discuss Juvenile dermatomyositis. Click on the link to go to OMIM and review these resources.
- Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.
- PubMed is a searchable database of medical literature and lists journal articles that discuss Juvenile dermatomyositis. Click on the link to view a sample search on this topic.