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Hae accounts for only a small fraction of all cases of angioedema While current treatment options may have vastly improved life with hae, many are still impacted by the disease. To avoid potentially fatal consequences such as upper airway obstruction and unnecessary abdominal surgery, the importance of a correct diagnosis cannot be overemphasized.

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Hereditary angioedema (hae) is a rare, genetic disorder that causes episodes of swelling in the face, hands, feet and elsewhere Living with hereditary angioedema (hae) often means living with mild attacks and regular accommodations Symptoms usually begin in childhood.

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Hereditary angioedema is a rare genetic condition that causes swelling under the skin and lining of the gut and lungs

It can happen in different parts of your body You are born with hereditary. Our association is a community of people affected by hae and their loved ones who are leading the fight in hae research, advocacy and finding a cure. Hae symptoms include episodes of edema (swelling) in various body parts including the hands, feet, face and airway.

Hereditary angioedema (hae) is a disease characterized by recurrent episodes of angioedema, without urticaria (also called wheals) or pruritus, which most often affect the skin or mucosal tissues of the upper respiratory and gastrointestinal tracts. The most common cause of hae is a decrease in c1 esterase inhibitor (c1 inh), a protein that is part of our body’s normal immune system A peptide called bradykinin is thought to be responsible for the hae symptoms of swelling, inflammation and pain. The symptoms of hereditary angioedema (hae) include recurring swelling in different areas of the body

Early signs of an attack may be tingling and a rash, followed by swelling in the affected area

Hae attacks can be unpredictable and vary by person. Hereditary angioedema (hae) is a rare genetic condition