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Hereditary Angioedema

Hereditary angioedema (HAE) is a rare genetic disorder caused by a deficiency of a blood protein called C1-INH.  Symptoms of HAE may include swelling of the hands, face, feet, abdomen and throat. Attacks of HAE typically have a rapid onset, and symptoms may subside gradually over 3 to 5 days.

Deaconess Clinic Department of Allergy and Immunology is participating in a clinical research study of an investigational medication for the prevention of HAE attacks. Qualified participants receive study-related medical care at no cost.

If you are interested in learning more about this study, please call the Deaconess Research InfoLine at 812-474-7184 or toll free 877-654-0311.
 
Research Physicians:
Dr. Majed Koleilat, Dr. Anne McLaughlin, Dr. Jason White

 

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