World-wide medical news for clinical use. Contributions edited by Dr.A.Franklin MBBS(Lond)Dip.Phys.Med (UK) DPH & DIH(Tor.)LMC(C) FLEx(USA) Fellow Med.Soc.London
11 October 2013
USA "GARD": HEREDITARY ANGIOEDEMA
Who first described hereditary angioedema?
Hereditary angioedema (HAE) was first described as a “syndrome” by Quincke in 1882 and was later detected in 1888 by William Osler to have a hereditary nature.[1]
1. Webb, M. et al. 2000. Management of children with hereditary angioedema: a report of two cases. Available at: http://www.aapd.org/assets/1/25/Webb-22-02.pdf. Accessed on October 11, 2013.
The US Hereditary Angioedema Association
Seven Waterfront Plaza
500 Ala Moana Blvd., Suite 400
Honolulu, HI 96813
Toll free: (866) 798-5598
Web site: http://www.haea.org/
Tamandra Carter
Information Specialist
The Genetic and Rare Diseases (GARD) Information Center is funded by two parts of the National Institutes of Health (NIH): the National Center for Advancing Translational Sciences Office of Rare Diseases Research (NCATS-ORDR) and the National Human Genome Research Institute (NHGRI). The GARD Information Center provides the public with access to current, reliable, and easy to understand information about rare or genetic diseases in English or Spanish. Information Specialists are available by phone Monday through Friday, 12:00 p.m. to 6:00 p.m. Eastern time (excluding Federal holidays).
PO Box 8126
Gaithersburg, MD 20898-8126
Toll-free: 1-888-205-2311
Telephone: 301-251-4925
TTY: 1-888-205-3223
Fax: 301-251-4911
E-mail: GARDinfo@nih.gov
Web site: http://rarediseases.info.nih.gov/GARD
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