[Home ] [Archive]    
:: Main About journal Editorial Board Current Issue Archive Submit an article Site Map Contact ::
Main Menu
Home::
Journal Information::
Articles archive::
For Authors::
For Reviewers::
Registration::
Contact us::
Site Facilities::
Editorial Board::
::
Search in website

Advanced Search
..
Receive site information
Enter your Email in the following box to receive the site news and information.
..
:: Volume 2, Issue 2 (June 2013) ::
Int J Med Invest 2013, 2(2): 0-0 Back to browse issues page
HEREDITARY ANGIOEDEMA
Aslan Ozgur * , Kavalci Cemil , Ozlem Miray , Kavalci Gülsüm , Ceyhan Mehmet Ali , Yilmaz Fevzi
Numune Training and Research Hospital, Emergency department, Ankara/Turkey
Abstract:   (8345 Views)
Hereditary angioedema (HAE) is a extremely rare disease, which is caused by deficiency or dysfunction of C1-esterase inhibitor. A 28 year old woman presented to emergency department with edema at face, eyes and around the mouth and tongue. Antihistaminic and corticosteroid were given again after monitorization of the patient. Fresh frozen plasma was given at a dose of 10 ml/kg. She was discharged after resolution of complaints during the follow-up period.
Full-Text [PDF 516 kb]   (2313 Downloads)    
Type of Study: case report | Subject: General
Add your comments about this article
Your username or Email:

CAPTCHA


XML     Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Ozgur A, Cemil K, Miray O, Gülsüm K, Mehmet Ali C, Fevzi Y. HEREDITARY ANGIOEDEMA. Int J Med Invest 2013; 2 (2)
URL: http://intjmi.com/article-1-34-en.html


Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
Volume 2, Issue 2 (June 2013) Back to browse issues page
International Journal of Medical Investigation
Persian site map - English site map - Created in 0.05 seconds with 36 queries by YEKTAWEB 4645