National Organization for Rare Disorders, Inc.Epidermolysis BullosiaImportant It is possible that the main title of the report Epidermolysis Bullosia 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- epidermolysis bullosa simplex
- junctional epidermolysis bullosa
- dystrophic epidermolysis bullosa
General DiscussionEpidermolysis bullosa (EB) is a genetic skin disorder characterized clinically by blister formation from mechanical trauma. There are three main types with additional sub-types identified. There is a spectrum of severity, and within each type, one may be either mildly or severely affected. EB ranges from being a minor inconvenience requiring modification of some activities, to being completely disabling and, in some cases, fatal.
Friction causes blister formation. Blisters can form anywhere on the surface of the skin, within the oral cavity and in more severe forms may also involve the external surface of the eye, as well as the respiratory, gastrointestinal and genitourinary tracts. In some forms of the disease, disfiguring scars and disabling musculoskeletal deformities occur.
Currently, there is no cure for EB. Supportive care includes daily wound care, bandaging, and pain management as needed ResourcesDystrophic Epidermolysis Bullosa Research Association of America, Inc. (DEBRA) 16 East 41st Street Third Floor New York, NY 10017 Tel: (212)868-1573 Fax: (212)868-9296 Tel: (866)332-7276 Email: staff@debra.org Internet: http://www.debra.org
DebRA 13 Wellington Business Park Dukes Ride Crowthorne Berkshire, RG45 6LS United Kingdom Tel: +44 1344 771961 Fax: 44 1344 762661 Email: debra@debra.org.uk Internet: http://www.debra.org.uk
EB Medical Research Foundation 8909 W. Olympic Blvd. #222 Beverly Hills, CA 90211 Tel: (310)854-0957 Email: a.pett@bep-la.com Internet: http://www.ebkids.org
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/
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
Epidermolysis Bullosa Action Network (EBAN, Inc.) 16613 Milan De Avila Tampa, FL 33613 Tel: (813)325-1955 Email: silvia@ebanusa.org Internet: http://www.ebanusa.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: 4/28/2009 Copyright 1984, 1985, 1986, 1987, 1988, 1989, 1990, 1991, 1992, 1993, 1994, 1995, 1996, 1997, 1999, 2002, 2005, 2006, 2007, 2008, 2009 National Organization for Rare Disorders, Inc.
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