Scientific and clinical progress together with the development of effective novel therapeutic
options has engendered multiple important changes in the diagnosis and management of …

These parameters were developed by the Joint Task Force on Practice Parameters (JTFPP),
representing the American Academy of Allergy, Asthma & Immunology (AAAAI); the …

BACKGROUND: Hereditary angioedema due to C1 inhibitor deficiency (HAE-C1-INH) is
characterized by relapsing skin swellings, abdominal pain attacks, and, less frequently …

A 19-year-old woman presents to the emergency department with light-headedness, severe
abdominal pain, and intractable nausea and vomiting that began 12 hours earlier. The …

PURPOSE: Hereditary angioedema (HAE) due to C1 inhibitor deficiency is clinically
characterized by relapsing skin swellings, abdominal pain attacks, and life-threatening …

▪ Objective: To review available information on cough and angioneurotic edema associated
with angiotensin-converting enzyme (ACE) inhibitors.▪ Data Sources: All relevant articles …

Abstract Background We published the Canadian 2003 International Consensus Algorithm
for the Diagnosis, Therapy, and Management of Hereditary Angioedema (HAE; C1 inhibitor …

Background Bradykinin is believed to be the main mediator of symptoms in hereditary (HA)
and acquired (AA) angio-oedema due to C1 esterase inhibitor deficiency, as well as in angio …

Hereditary angioedema (HAE), a rare but life-threatening condition, manifests as acute
attacks of facial, laryngeal, genital, or peripheral swelling or abdominal pain secondary to …

Background Hereditary angioedema due to C1 inhibitor deficiency is characterized by
recurrent acute attacks of swelling that can be painful and sometimes life-threatening …