National Organization for Rare Disorders, Inc.Marfan SyndromeImportant It is possible that the main title of the report Marfan Syndrome 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.
SynonymsDisorder Subdivisions- Marfan Syndrome Type I
- Marfan Syndrome Type II
General DiscussionMarfan syndrome is a genetic disorder that affects connective tissue, which is the material between cells of the body that gives the tissues form and strength. Connective tissue is found all over the body and multiple organ systems may be affected in individuals with Marfan syndrome. The heart and blood vessels (cardiovascular), skeletal, and eye (ocular) systems are most often affected. Major symptoms include overgrowth of the long bones of the arms and legs, abnormal side-to-side curvature of the spine (scoliosis), indentation or protrusion of the chest wall (pectus), dislocation of the lenses of the eyes (ectopia lentis), nearsightedness (myopia), widening (aneurysm) and degeneration of the main artery that carries blood away from the heart (aorta), floppiness of the mitral valve (mitral valve prolapse) and backward flow of blood through the aortic and mitral valves (aortic and mitral regurgitation). The specific symptoms and the severity of Marfan syndrome vary greatly from case to case. Marfan syndrome is inherited as an autosomal dominant trait. Defects or disruptions (mutations) of the fibrillin-1 (FBN1) gene have been linked to Marfan syndrome and related disorders. ResourcesMarch 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
National Marfan Foundation 22 Manhasset Avenue Port Washington, NY 11050 Tel: (516)883-8712 Fax: (516)883-8040 Tel: (800)862-7326 Email: staff@marfan.org Internet: http://www.marfan.org
NIH/National Arthritis and Musculoskeletal and Skin Diseases Information Clearinghouse 1 AMS Circle Bethesda, MD 20892-3675 USA Tel: (301)495-4484 Fax: (301)718-6366 Tel: (877)226-4267 TDD: (301)565-2966 Email: NIAMSinfo@mail.nih.gov Internet: http://www.niams.nih.gov/Health_Info
Marfan Association UK Rochester House 5 Aldershot Road Fleet Hampshire, GU51 3NG United Kingdom Tel: +44 (0) 1252 810472 Fax: +44 (0) 1252 810473 Email: marfan@tinyonline.co.uk Internet: http://www.marfan-association.org.uk/
Canadian Marfan Association Centre Plaza Postal Outlet 128 Queen Street South P.O. Box 42257 Mississauga Ontario, L5M 4Z0 Canada Tel: 9058263223 Fax: 9058262125 Tel: 8667221722 Email: info@marfan.ca Internet: http://www.marfan.ca
MUMS National Parent-to-Parent Network 150 Custer Court Green Bay, WI 54301-1243 USA Tel: (920)336-5333 Fax: (920)339-0995 Tel: (877)336-5333 Email: mums@netnet.net Internet: http://www.netnet.net/mums/
Sjældne Diagnoser / Rare Disorders Denmark Frederiksholms Kanal 2, 3rd Floor Copenhagen K, 1220 Denmark Tel: 45 33 14 00 10 Fax: 45 33 14 55 09 Email: mail@sjaeldnediagnoser Internet: http://www.raredisorders.dk
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 Email: ordr@od.nih.gov Internet: http://rarediseases.info.nih.gov/Default.aspx
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
Let Them Hear Foundation 1900 University Avenue, Suite 101 East Palo Alto, CA 94303 Tel: (650)462-3143 Fax: (650)462-3144 Tel: (877)735-2929 Email: info@letthemhear.org Internet: http://www.letthemhear.org
For a Complete ReportThis 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: 2/5/2008 Copyright 1984, 1985, 1987, 1988, 1989, 1990, 1992, 1994, 1995, 1997, 1999, 2002, 2003, 2007, 2008 National Organization for Rare Disorders, Inc.
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