Hereditary angioedema (HAE) due to C1-inhibitor (C1-INH) deficiency or dysfunction is a
rare genetic disorder that causes recurrent episodes of swelling in various parts of the body …

Hereditary angioedema (HAE) is an uncommon disorder characterized clinically by
recurrent episodes of nonitchy subcutaneous and/or submucosal swellings. The estimated …

Background Urticaria (defined as the presence of hives, angioedema, or both) can be
caused by a variety of etiologies ranging from more common conditions such as chronic …

Introduction Olfactory dysfunction (OD) is common among patients with chronic
rhinosinusitis (CRS). Validated and culturally specific tests, such as the “Sniffin'Sticks” test …

Background Hereditary angioedema (HAE) is a rare genetic disease. Patients with type II
HAE have normal or elevated C1-inhibitor (C1-INH) levels but C1-INH protein is …

Background With no approved long-term prophylaxis (LTP) for the prevention of hereditary
angioedema (HAE) attacks in Hong Kong, patients rely on compassionate use programs …

Introduction and objectives Due to the lack of structured and systematic information
available, the aim of this study was to describe the epidemiology, diagnosis, healthcare …

Bradykinin-mediated angioedema can broadly be categorised into hereditary angioedema
(HAE) and acquired angioedema (AAE). Both HAE and AAE are grossly under-recognised …

Conclusions• Sebetralstat PK, PD, and safety profiles were comparable in healthy
Japanese, Chinese, and White adults• Near-complete (≥ 95% geometric mean) inhibition of …

The Asia Pacific Association of Allergy, Asthma and Clinical Immunology (APAAACI) is the
regional allergy organization of Asia Pacific. It aims to advance impact and communicate all …