Results 101 to 110 of about 111,576 (246)

Angioedema

Allergy, Asthma & Clinical Immunology
Angioedema can occur in the absence of urticaria and can be broadly divided into three main categories: mast cell-mediated (e.g., histamine), non-mast-cell-mediated (bradykinin-induced) and idiopathic angioedema.
Gina Lacuesta, Stephen D. Betschel, Ellie Tsai, Harold Kim   +3 more
doaj   +1 more source

A Cohort Study on Incidence and Factors Associated With Adverse Drug Reactions of Enalapril in Lusaka, Zambia

Pharmacology Research &Perspectives, Volume 14, Issue 5, October 2026.
ABSTRACT Angiotensin‐converting enzyme inhibitors (ACEIs) are widely prescribed but are associated with adverse drug reactions (ADR), including angioedema, which is typically reported in 0.1%–0.7%. Data from sub‐Saharan Africa are limited. This study aimed to estimate the incidence and risk factors of enalapril‐associated ADRs in a Zambian cohort, with
Ntemena Yikon'a, Ngosa Mumba, Sarah Pedretti, Helen Hoenck, Jonathan Peter, Owen Ngalamika   +5 more
wiley   +1 more source

Probable “Escitalopram induced” angioedema in a patient with hereditary angioedema [PDF]

, 2019
Hereditary angioedema is an autosomal dominant disorder. Considerable rate of mortality determines the importanceof disease. In this paper, a patient with HAE who developed severe facial angioedema after the first dose of an antidepressant prescribed by ...
YıIdız, Eray, Aytekin, Gökhan, Arslan, Şevket, Çalışkaner, Ahmet Zafer, Çölkesen, Fatih   +4 more
core   +1 more source

Elevated level of circulating VEGF in Chinese patients with hereditary angioedema and its correlation with disease status

Orphanet Journal of Rare Diseases
Background Hereditary angioedema (HAE) is a rare inherited disease characterized by recurrent, potentially life-threatening angioedema. The vascular endothelium dysfunction is reported to play a role in angioedema episodes.
Ruoyu Ji, Yijing Xu, Yuxiang Zhi
doaj   +1 more source

Successful anesthetic management during abdominal wall-lifting laparoscopic cholecystectomy in a patient with hereditary angioedema

JA Clinical Reports, 2018
Background Hereditary angioedema is a rare genetic disorder resulting from an inherited deficiency or dysfunction of the C1-esterase inhibitor. In the anesthetic management of such patients, special caution should be exercised while attempting tracheal ...
Masashi Fujii, Takayuki Higashiguchi, Nobuaki Shime, Yasuyo Kawabata   +3 more
doaj   +1 more source

Food Allergy Incidence Among Hong Kong Children From 2005 to 2024

Clinical &Experimental Allergy, EarlyView.
Christy Wing Man Leung, Michal Ordak, Nam Sze Cheng, Ting Fan Leung   +3 more
wiley   +1 more source

Chronic Spontaneous Urticaria and Psychiatric Symptoms: The Blood–Brain Barrier Hypothesis

Experimental Dermatology, Volume 35, Issue 10, October 2026.
ABSTRACT Chronic spontaneous urticaria (CSU) is a mast cell‐driven inflammatory disease frequently accompanied by anxiety, depression, sleep disturbance, fatigue, and impaired quality of life. Pruritus, disturbed sleep, psychosocial burden, and treatment‐related effects are established contributors to this neuropsychiatric and functional burden ...
Gerasimos N. Konstantinou, Jerry J. Warsh, Daniel M. Blumberger, Stefan Kloiber, George N. Konstantinou   +4 more
wiley   +1 more source

Diagnosis and screening of patients with hereditary angioedema in primary care

, 2016
Maria Paula Henao,1 Jennifer L Kraschnewski,1 Theodore Kelbel,2 Timothy J Craig3 1Department of Medicine, 2Division of Allergy and Immunology, 3Department of Medicine and Pediatrics, Pennsylvania State University College of Medicine at Hershey Medical ...
Craig TJ, Kelbel T, Kraschnewski JL, Henao MP   +3 more
core  

Position statement of the hereditary angioedema Section of the Polish Society of Allergology on the management of hereditary angioedema due to C1 inhibitor deficiency: 2025 update. Part I: Classification, pathophysiology, clinical presentation, diagnosis, and differential diagnosis

Hereditary angioedema due to a genetically determined deficiency of the C1 complement inhibitor (HAE-C1INH) is a rare disease that significantly impairs daily functioning and may be life-threatening in severe cases.
Jacek Gocki, Małgorzata Sokołowska, Mateusz Łukaszyk, Marta Tykwińska, Grzegorz Porębski, Aleksandra Kucharczyk, Tomasz Matuszewski, Aldona Juchacz, Hanna Danielewicz, Ewa Trębas-Pietraś, Krzysztof Kuziemski, Katarzyna Grzela, Marcin Stobiecki, Marcin Kurowski, Krystyna Obtułowicz   +14 more
core   +1 more source

Epidemiology of Non-hereditary Angioedema

, 2012
The prevalence of non-hereditary angioedema was investigated in a general population sample (n¿=¿7,931) and in a sample of Danish patients (n¿=¿7,433) tested for deficiency of functional complement C1 esterase inhibitor protein (functional C1 INH).
Attermann, Jørn, Linneberg, Allan, Madsen, Flemming   +2 more
core   +1 more source