National Organization for Rare Disorders, Inc.
It is possible that the main title of the report Sydenham Chorea is not the name you expected.
Sydenham chorea is a rare neurological disorder characterized by rapid, involuntary, purposeless movements, especially of the face, feet and hands. Additional symptoms may include muscle weakness and emotional or behavioral problems. Sydenham chorea most often affects children and adolescents. Sydenham chorea usually develops following Streptococcal infection and may occur as an isolated finding or as a major complication of acute rheumatic fever. The movement disorder is considered an autoimmune disorder, meaning it occurs when the body's immune system (which normally responds to a foreign substance) mistakenly attacks healthy tissue.
Centers for Disease Control and Prevention
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Genetic and Rare Diseases (GARD) Information Center
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Movement Disorder Society
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- Suite 1100
- Milwaukee, WI 53202-3823
- Tel: (414)276-2145
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- Website: http://www.movementdisorders.org
NIH/National Institute of Neurological Disorders and Stroke
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- Website: http://www.ninds.nih.gov/
For a Complete Report
This is an abstract of a report from the National Organization for Rare Disorders (NORD). For a full-text version of this report, go to www.rarediseases.org and click on Rare Disease Database under "Rare Disease Information".
The information provided in this report is not intended for diagnostic purposes. It is provided for informational purposes only.
It is possible that the title of this topic is not the name you selected. Please check the Synonyms listing to find the alternate name(s) and Disorder Subdivision(s) covered by this report.
This disease entry is based upon medical information available through the date at the end of the topic. Since NORD's resources are limited, it is not possible to keep every entry in the Rare Disease Database completely current and accurate. Please check with the agencies listed in the Resources section for the most current information about this disorder.
Last Updated: 2/22/2010
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