Results 11 to 20 of about 616 (213)

A case of angioedema of hereditary origin in a rural clinic near Subotica [PDF]

ABC: časopis urgentne medicine, 2023
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, Momirović-Stojković Milena, Budimski-Soldat Mihaela   +2 more
doaj   +3 more sources

Prevalence of autoantibodies in a group of hereditary angioedema patients Prevalência de autoanticorpos em uma população com angioedema hereditário [PDF]

Anais Brasileiros de Dermatologia, 2012
Hereditary Angioedema is a dominantly inherited disease. Routine screening of autoantibodies (AAB) is not recommended for individuals with Hereditary Angioedema; however, prevalence of these antibodies in Hereditary Angioedema patients is not well ...
Sergio Duarte Dortas Junior, Solange Oliveira Rodrigues Valle, Soloni Afra Pires Levy, Rosangela P. Tortora, Augusto Tiaqui Abe, Gisele Viana Pires, José Angelo de Souza Papi, Alfeu Tavares França   +7 more
doaj   +2 more sources

Hereditary angioedema type III (estrogen-dependent) report of three cases and literature review* [PDF]

Anais Brasileiros de Dermatologia, 2013
In this article, three cases of hereditary angioedema (HAE) type III (estrogen-dependent or with normal C1 inhibitor) are reported. The HAE was initially described in women of the same family in association with high-leveled estrogenic conditions such as
Amanda Rodrigues Miranda, Ana Paula Fusel de Ue, Dominique Vilarinho Sabbag, Wellington de Jesus Furlani, Patrícia Karla de Souza, Osmar Rotta   +5 more
doaj   +2 more sources

Reply to “A Case Report about the Management of Hereditary Angioedema with Normal Complement Levels during Pregnancy” [PDF]

Acta Médica Portuguesa
N/A.
Ana Luísa Moura, Ângela Gaspar, Luís Miguel Borrego   +2 more
doaj   +3 more sources

Hereditary angioedema prevalence and satisfaction with prophylaxis in South Australia [PDF]

World Allergy Organization Journal
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, Karen Milburn, RN, Pravin Hissaria, MBBS, MD, Thanh Thao (Adriana) Le, MBBS, William Smith, MBBS, PhD   +4 more
doaj   +2 more sources

Complex analysis of the national Hereditary angioedema cohort in Slovakia – Identification of 12 novel variants in SERPING1 gene [PDF]

World Allergy Organization Journal
Background: Hereditary angioedema (HAE) is a rare autosomal dominant genetic disease characterised by acute episodes of non-pruritic skin and submucosal swelling caused by increase in vascular permeability.
Adam Markocsy, MD, Katarina Hrubiskova, MD, Martin Hrubisko, MD, PhD, Tomas Freiberger, MD, PhD, Hana Grombirikova, MSc, Lenka Dolesova, MSc, PhD, Ludmila Slivka Vavrova, MSc, PhD, Regina Lohajova Behulova, MSc, PhD, Martina Ondrusova, MSc, PhD, MPH, Peter Banovcin, MD, PhD, Karolina Vorcakova, MD, PhD, Milos Jesenak, MD, MSc, PhD, MBA, MHA, FAAAAI   +11 more
doaj   +2 more sources

Th2 predominance and decreased NK cells in patients with hereditary angioedema. [PDF]

Front Immunol
BackgroundIn this study we included patients with hereditary angioedema (HAE) caused by decreased levels of C1 inhibitor (HAE-C1INH). An increased risk of autoimmune disorders, particularly systemic lupus erythematosus (SLE), has been reported in HAE ...
Sundler Björkman L, Elmér E, Egesten A, Skattum L.   +3 more
europepmc   +3 more sources

Hereditary angioedema [PDF]

International Journal of Emergency Medicine, 2021
AbstractA 14-year-old African American female presented to the emergency department with spontaneous, sudden-onset lip swelling for 1 h. On examination, there was significant water-bag edema of the upper lip extending to the philtrum and premaxilla. Nasopharyngeal laryngoscopy revealed a patent airway without edema.
Helen Lesser, Jason E. Cohn
openaire   +4 more sources

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
  +5 more sources

Assessment of HAE prophylaxis transition from androgen therapy to berotralstat: A subset analysis of the APeX-S trial

World Allergy Organization Journal, 2023
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, Bhavisha Desai, PharmD, Dianne Tomita, MPH, Phil Collis, PhD, Marcin Stobiecki, MD, PhD   +4 more
doaj   +1 more source