The characteristics of upper airway edema in hereditary and acquired angioedema with C1‐inhibitor deficiency [PDF]
Background Angioedemas localized in the upper airway are potentially life threatening, and without proper treatment, they may lead to death by suffocation. Upper airway edemas (UAE) in bradykinin‐mediated angioedemas can even be the first symptoms of the
Zsuzsanna Balla +8 more
doaj +3 more sources
Angioedemas associated with renin-angiotensin system blocking drugs: Comparative analysis of spontaneous adverse drug reaction reports. [PDF]
IntroductionAngioedema is a subcutaneous swelling typically affecting the face, larynx or pharynx. It is a known adverse drug reaction (ADR) of ACE inhibitors (ACEi), angiotensin-II-receptor blockers (ARBs) and aliskiren (renin inhibitor).
Diana Dubrall +3 more
doaj +3 more sources
Over diagnosis of bradykinin angioedema in patients treated with angiotensin-converting enzyme inhibitors or angiotensin II receptor blockers [PDF]
Background: Bradykinin angioedemas are a potentially serious side effect of angiotensin-converting enzyme inhibitors (ACEI) and more controversially of angiotensin II receptor blockers (ARB).
Marie Douillard, MD +7 more
doaj +2 more sources
Screening for Plasminogen Mutations in Hereditary Angioedema Patients. [PDF]
Hereditary angioedema (HAE) is a rare disease belonging to the group of bradykinin-mediated angioedemas, characterized by recurring edematous episodes involving the subcutaneous and/or submucosal tissues.
Farkas H +4 more
europepmc +2 more sources
Pathophysiology of bradykinin and histamine mediated angioedema. [PDF]
Angioedema is characterized by swelling localized to the subcutaneous and submucosal tissues. This review provides an overview of angioedema, including the different types, triggers, and underlying pathophysiologic mechanisms.
Lima H +4 more
europepmc +2 more sources
Hereditary angioedema prevalence and satisfaction with prophylaxis in South Australia [PDF]
Background: Hereditary angioedema (HAE) due to deficiency of C1 Inhibitor (C1INH-HAE) is a rare, unpredictable and potentially fatal genetic disorder. There are relatively few systematic population prevalence studies, with reports from various countries ...
Alexander Troelnikov, MBBS +4 more
doaj +2 more sources
A case of angioedema of hereditary origin in a rural clinic near Subotica [PDF]
Introduction: Hereditary angioedema (HAE) is inherited in an autosomal dominant manner. It manifests with bradykinin-mediated swelling due to a deficiency of C1 inhibitor.
Gavrilović Nikola +2 more
doaj +1 more source
Long-term prophylaxis of hereditary angioedema [PDF]
Hereditary angioedema (HAE) is a rare inherited disease characterized by recurrent attacks of painful swelling of the subcutaneous and submucosal tissues.
Dijana Perković +8 more
doaj +1 more source
Background: Given the recent approval of oral berotralstat in several countries for hereditary angioedema (HAE) prophylaxis, transition from long-term androgens to berotralstat may occur in clinical practice.
Jonny G. Peter, MB ChB, MMed, FCP (SA), PhD +4 more
doaj +1 more source
This update and revision of the international guideline for urticaria was developed following the methods recommended by Cochrane and the Grading of Recommendations Assessment, Development and Evaluation (GRADE) working group. It is a joint initiative of
T. Zuberbier +66 more
semanticscholar +1 more source

