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Dysautonomia, Familial

National Organization for Rare Disorders, Inc.

Important
It is possible that the main title of the report Dysautonomia, Familial 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

  • FD
  • Hereditary Sensory and Autonomic Neuropathy, Type III (HSAN, Type III)
  • Hereditary Sensory Neuropathy Type III
  • HSAN-III
  • HSN-III
  • Riley-Day Syndrome

Disorder Subdivisions

  • None

General Discussion

Familial dysautonomia is a rare genetic disorder of the autonomic nervous system (ANS) that primarily affects people of Eastern European Jewish heritage. It is characterized by diminished sensitivity to pain, lack of overflow tearing in the eyes, a decrease in the number of knob-like projections that cover the tongue (fungiform papillae), unusual fluctuations of body temperature, and unstable blood pressure. Symptoms of this disorder are apparent at birth. The autonomic nervous system controls vital involuntary body functions.

Resources

Dysautonomia Foundation, Inc.
315 W 39th St
Suite 701
New York, NY 10018
USA
Tel: (212)279-1066
Fax: (212)279-2066
Email: info@famdys.org
Internet: http://www.familialdysautonomia.org

March of Dimes Birth Defects Foundation
1275 Mamaroneck Avenue
White Plains, NY 10605
Tel: (914)997-4488
Fax: (914)997-4763
Tel: (888)663-4637
Email: Askus@marchofdimes.com
Internet: http://www.marchofdimes.com

NIH/National Institute of Neurological Disorders and Stroke
P.O. Box 5801
Bethesda, MD 20824
Tel: (301)496-5751
Fax: (301)402-2186
Tel: (800)352-9424
TDD: (301)468-5981
Internet: http://www.ninds.nih.gov/

Dysautonomia Foundation, Inc., Toronto Chapter
250 Franklin Avenue
Thornhill
Ontario, L4J 7K5
Canada
Tel: 9058827725
Fax: 9057647752
Internet: http://www.familialdysautonomia.org

National Dysautonomia Research Foundation
PO Box 301
Red Wing, MN 55066-0102
Tel: (651)327-0367
Email: ndrf@ndrf.org
Internet: http://www.ndrf.org

Familial Dysautonomia Hope Foundation
121 S. Estes Dr., Suite 205D
Chapell Hill, NC 27514
USA
Tel: (919)969-1414
Email: info@fdhope.org
Internet: http://www.fdhope.org

Genetic and Rare Diseases (GARD) Information Center
PO Box 8126
Gaithersburg, MD 20898-8126
Tel: (301)251-4925
Fax: (301)251-4911
Tel: (888)205-2311
TDD: (888)205-3223
Internet: http://rarediseases.info.nih.gov/GARD/

Madisons Foundation
PO Box 241956
Los Angeles, CA 90024
Tel: (310)264-0826
Fax: (310)264-4766
Email: getinfo@madisonsfoundation.org
Internet: http://www.madisonsfoundation.org

Familial Dysautonomia Now Foundation
1170 Green Knolls Drive
Buffalo Grove, IL 60089
Tel: (847)913-0455
Fax: (847)913-8589
Email: fdnow@comcast.net
Internet: http://www.fdnow.org

Dysautonomia Youth Network of America, Inc.
1301 Greengate Court
Waldorf, OR 20601
Tel: (301)705-6995
Fax: (301)638-3962
Email: info@dynakids.org
Internet: http://www.dynakids.org

For a Complete Report

This is an abstract of a report from the National Organization for Rare Disorders (NORD). A copy of the complete report can be downloaded free from the NORD website for registered users. The complete report contains additional information including symptoms, causes, affected population, related disorders, standard and investigational therapies (if available), and references from medical literature. For a full-text version of this topic, 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. 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:  8/17/2007
Copyright  1985, 1986, 1988, 1990, 1991, 1993, 1999, 2001, 2002, 2007 National Organization for Rare Disorders, Inc.

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