National Organization for Rare Disorders, Inc.
It is possible that the main title of the report Machado-Joseph Disease is not the name you expected.
Machado-Joseph Disease (MJD-III), also called spinocerebellar ataxia type III, is a rare, inherited, ataxia (lack of muscular control) affecting the central nervous system and characterized by the slow degeneration of particular areas of the brain called the hindbrain. Patients with MJD may eventually become crippled and/or paralyzed but their intellect remains intact. The onset of symptoms of MJD varies from early teens to late adulthood.
Three forms of Machado-Joseph Disease are recognized: Types MJD-I, MJD-II, and MJD-III. The differences in the types of MJD relate to the age of onset and severity. Earlier onset usually produces more severe symptoms.
Genetic and Rare Diseases (GARD) Information Center
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International Joseph Disease Foundation, Inc.
- P.O. Box 994268
- Redding, CA 96099
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NIH/National Institute of Neurological Disorders and Stroke
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- Website: http://www.ninds.nih.gov/
National Ataxia Foundation
- 2600 Fernbrook Lane Suite 119
- Minneapolis, MN 55447
- Tel: (763)553-0020
- Fax: (763)553-0167
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- Website: http://www.ataxia.org
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.
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Last Updated: 5/23/2008
Copyright 2003 National Organization for Rare Disorders, Inc.
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