Results 21 to 30 of about 20,541 (234)

Mutational spectrum and genotype-phenotype relationships in a cohort of Romanian hereditary angioedema patients caused by C1 inhibitor deficiency

Romanian Journal of Laboratory Medicine, 2019
Background: Hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE) caused by SERPING1 mutations is a rare monogenic disorder characterized by a high frequency of de novo mutations, allelic heterogeneity and populational differences.
Gábos Gabriella, Moldovan Dumitru, Dobru Daniela, Mihály Enikő, Bara Noémi, Nădășan Valentin, Hutanu Adina, Csép Katalin   +7 more
doaj   +1 more source

Angioedema. Interdisciplinary diagnostic and therapeutic recommendations of the Polish Dermatological Society (PTD) and Polish Society of Allergology (PTA)

Przegląd Dermatologiczny, 2020
Angioedema is a non-inflammatory edema of the subcutaneous tissue and/or mucosal membranes. It commonly coexists with urticaria and is considered a deep form of urticaria.
Roman Nowicki, Elżbieta Grubska-Suchanek, Grzegorz Porębski, Marek L. Kowalski, Karina Jahnz-Różyk, Tomasz Matuszewski, Lidia Rudnicka, Marek Kulus, Wioletta Barańska-Rybak, Rafał Czajkowski, Zbigniew Doniec, Cezary Kowalewski, Beata Kręcisz, Magdalena Lange, Joanna Narbutt, Małgorzata Olszewska, Małgorzata Sokołowska-Wojdyło, Aneta Szczerkowska-Dobosz, Radosław Śpiewak, Magdalena Trzeciak, Aleksandra Wilkowska   +20 more
doaj   +1 more source

A patient with hereditary angioedema and systemic lupus erythematosus: Coincidence or coexistence?

Medicine Science, 2020
Angioedema is classified into two major groups: mast cell-mediated (histaminergic) and bradykinin-mediated angioedema. Hereditary angioedema and acquired angioedema are well-defined groups of bradykinin-mediated angioedema. Both hereditary angioedema and
Gokhan Aytekin, Fatih Colkesen, Eray Yildiz, Sevket Arslan   +3 more
doaj   +1 more source

Hospitalizations due to Angioedema without Urticaria in a Portuguese Center: Five Year Retrospective Study

Acta Médica Portuguesa, 2019
Introduction: Hospitalizations due to angioedema are important especially in debilitating or life-threatening situations. The aim of this study was to evaluate the frequency and etiology of angioedema without urticaria in hospital admissions.
Joana Cosme, Amélia Spínola, Manuel Branco Ferreira, Manuel Pereira Barbosa   +3 more
doaj   +1 more source

ACE inhibitor angioedema: characterization and treatment versus non-ACE angioedema in acute hospitalized patients

Journal of Community Hospital Internal Medicine Perspectives, 2020
Background ACE angioedema has not been characterized in comparison with angioedema from other causes in acute hospitalized patients. Methods We retrospectively compared ACE-angioedema and non-ACE angioedema patients from January 2013 to May 2017. Results
David S. Weisman, Nelly Arnouk, M. Bilal Asghar, M. Raheel Qureshi, Anagha Kumar, Sameer Desale, Lyn Camire, Stephen Pineda   +7 more
doaj   +1 more source

Over diagnosis of bradykinin angioedema in patients treated with angiotensin-converting enzyme inhibitors or angiotensin II receptor blockers

World Allergy Organization Journal, 2023
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, Zineb Deheb, MD, Agathe Bozon, MD, Nadia Raison-Peyron, MD, Olivier Dereure, MD, PhD, Lionel Moulis, MD, Angèle Soria, MD, PhD, Aurélie Du-Thanh, MD, PhD   +7 more
doaj   +1 more source

Subcutaneous C1‐Inhibitor Concentrate for prophylaxis during pregnancy and lactation in a patient with C1‐INH‐HAE

Clinical Case Reports, 2021
Subcutaneous plasma‐derived human C1‐Inhibitor concentrate (pdC1INH) may be safe and effective for long‐term prophylaxis during pregnancy and lactation in hereditary angioedema patients.
Shimalee Andarawewa, Emel Aygören‐Pürsün   +1 more
doaj   +1 more source

Early diagnosis of hereditary angioedema in children: genetic testing should be prioritized

Allergy, Asthma & Clinical Immunology
Background When a member of a family has been diagnosed with hereditary angioedema (HAE) before a child is born, the question of early diagnosis arises. Indeed, the first attacks may occur at birth.
A. Bocquet, A. Pagnier, I. Boccon-Gibod, F. Defendi, C. Dumestre-Perard, G. Hardy, Laurence Bouillet   +6 more
doaj   +1 more source

Terrible APS — a newly defined variant of severe APS

Frontiers in Immunology
IntroductionAntiphospholipid syndrome (APS) presents with various clinical features and some patients exhibit progressive, refractory disease that does not meet the catastrophic APS (cAPS) criteria. This study describes a new subcategory of APS patients,
Stanley Niznik, Tania Zaher, Tania Zaher, Soad Haj Yehia, Soad Haj Yehia, Ronen Shavit, Ronen Shavit, Shiri Weinstein, Yulia Lifshitz, Nancy Agmon-Levin, Nancy Agmon-Levin   +10 more
doaj   +1 more source

Hereditary Angioedema

Cureus, 2023
The authors present the case of a 22-year-old female who reported having a persistent sore throat. The patient had a history of recurring episodes of hereditary angioedema and arrived at the emergency department with her C1-esterase inhibitor. The epidemiology, clinical presentation, and treatment strategies are presented.
Banerjee, Anjali, Bermudez, Natalie, Gould, Murdoc B, Ramlatchan, Sidhartha R, Ganti, Latha   +4 more
openaire   +2 more sources