Results 91 to 100 of about 144,374 (198)
Chemotherapy in patients with hereditary angioedema
, 2018 Hereditary angioedema (HAE) is an autosomal dominant hereditary disorder characterized by episodic swelling of many body regions (especially throat and abdomen), potentially triggered by medication.
Guarino M. D. +6 more
core +1 more source
Vasculopathy: a possible factor affecting hereditary angioedema
Bleeding, Thrombosis and Vascular BiologyHereditary angioedema (HAE) is a rare genetic disorder that causes swelling of tissues in the hands, feet, limbs, face, intestinal tract, or airway. The SERPING1 gene, encoding the C1-INH, determines the wide range of clinical symptoms associated with ...
Anna Laura Colia +6 more
doaj +1 more source
Hereditary angioedema (HAE) in patients with C1 inhibitor deficiency : Cracow register [PDF]
, 2005 102 patients suffering from hereditary angioedema (HAE) belonging to 41 families have been studied. 96 patients (95.1%) had type I HAE characterized by low antigenic level and low functional activity of C1 inhibitor. 6 patients (4.9%) had type II HAE
Kapusta, Maria +2 more
core
Intestinal Angioedema Misdiagnosed as Recurrent Episodes of Gastroenteritis
Western Journal of Emergency Medicine, 2010 Emergency physicians (EP) frequently encounter angioedema involving the lips and tongue. However, angioedema from Angiotensin Converting Enzyme inhibitors or hereditary angioedema (HAE) can present with gastrointestinal symptoms due to bowel wall ...
LoCascio, Edward J +2 more
doaj
Completion of the Icatibant Outcome Survey and What We Learned
Clinical &Experimental Allergy, Volume 56, Issue 7, Page 784-787, July 2026.
Laurence Bouillet +8 more
wiley +1 more source
Screening for hereditary angioedema (HAE) at 13 emergency centers in Osaka, Japan
Medicine, 2017 Hereditary angioedema (HAE) with deficiency of C1 inhibitor (C1-INH) is an autosomal-dominant disease characterized by recurrent episodes of potentially life-threatening angioedema. The objective is to study the incidence of HAE among patients who visit the emergency department.This was a 3-year prospective observational screening study involving 13 ...
Hirose, Tomoya +14 more
openaire +2 more sources
Hereditary angioedema (HAE) is an autosomal dominantly inherited disease caused by deficiency of C1 esterase inhibitor protein type 1 (about 85% of patients with HAE-C1-INH) or type 2 oedema (about 15% of patients with HAE-C1-INH) by C1 inhibitor ...
Szymon Dyguś +6 more
core +1 more source
The Pathophysiology of Hereditary Angioedema [PDF]
, 2010 Hereditary angioedema (HAE) causes recurrent episodes of angioedema that may be very severe and are frequently associated with significant morbidity and even mortality. Understanding the pathophysiology of this disease is crucial for proper diagnosis and
Bruce L. Zuraw +2 more
core +1 more source
Research Progress on the Risk of Venous Thromboembolism in Patients with Hereditary Angioedema
罕见病研究Hereditary angioedema (HAE) is a hereditary disease characterized by recurrent cutaneous and/or submucosal edema. In recent years, it has also been observed that patients with HAE have an increased risk of developing venous thromboembolism (VTE).
JIANG Siqi, ZHI Yuxiang
doaj +1 more source
Real-world experience of hereditary angioedema (HAE) in Mexico: A mixed-methods approach to describe epidemiology, diagnosis, and treatment patterns. [PDF]
World Allergy Organ J, 2023 Nieto S +3 more
europepmc +1 more source