Subacute Sclerosing Panencephalitis


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Important

It is possible that the main title of the report Subacute Sclerosing Panencephalitis is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report.


Synonyms


  • Panencephalitis, Subacute Sclerosing
  • SSPE
  • Dawson's Disease
  • Dawson's Encephalitis

Disorder Subdivisions


  • None

General Discussion


Subacute sclerosing panencephalitis (SSPE) is a progressive neurological disorder characterized by inflammation of the brain (encephalitis). The disease may develop due to reactivation of the measles virus or an inappropriate immune response to the measles virus. SSPE usually develops 2 to 10 years after the original viral attack. Initial symptoms may include memory loss, irritability, seizures, involuntary muscle movements, and/or behavioral changes, leading to neurological deterioration.


Resources


Transverse Myelitis Association

1787 Sutter Parkway

Powell, OH 43065-8806

USA

Tel: 6147661806

Email: ssiegel@myelitis.org

Internet: http://www.myelitis.org



NIH/National Institute of Allergy and Infectious Diseases

6610 Rockledge Drive

MSC 6612

Bethesda, MD 20892-6612

Tel: (301)496-5717

Fax: (301)402-3573

TDD: (800)877-8339

Internet: http://www.niaid.nih.gov/



Encephalitis Global

1638 Pierard Road

North Vancouver

British Columbia, Intl V7J 1Y2

Canada

Tel: 604-980-2236

Fax: 6049040809

Email: wendystation@shaw.ca

Internet: http://www.encephalitisglobal.com



Encephalitis Society

7B Saville Street

Malton, North Yorkshire, YO17 7LL

UK

Tel: 44 (0) 1652 625 583

Email: mail@encephalitis.info

Internet: http://www.encephalitis.info




For a Complete Report


This is an abstract of a report from the National Organization for Rare Disorders, Inc. ® (NORD). A copy of the complete report can be obtained for a small fee by visiting the NORD website. The complete report contains additional information including symptoms, causes, affected population, related disorders, standard and investigational treatments (if available), and references from medical literature. For a full-text version of this topic, see http://www.rarediseases.org/search/rdblist.html

The information provided in this report is not intended for diagnostic purposes. It is provided for informational purposes only. NORD recommends that affected individuals seek the advice or counsel of their own personal physicians.

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.

For additional information and assistance about rare disorders, please contact the National Organization for Rare Disorders at P.O. Box 1968, Danbury, CT 06813-1968; phone (203) 744-0100; web site www.rarediseases.org or email orphan@rarediseases.org

Last Updated:   9/23/2005

Copyright   1986, 1987, 1994, 2003 National Organization for Rare Disorders, Inc.


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Last updated: September 23, 2005

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