Hereditary Angioedema
Mostrando 1-12 de 28 artigos, teses e dissertações.
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1. Icatibant use in Brazilian patients with hereditary angioedema (HAE) type 1 or 2 and HAE with normal C1-INH levels: findings from the Icatibant Outcome Survey Registry Study
Abstract Background: Hereditary angioedema can be caused by C1-Inhibitor (C1-INH) deficiency and/or dysfunction (HAE-1/2) or can occur in patients with normal C1-INH (HAE nC1-INH). Methods: The Icatibant Outcome Survey (IOS; NCT01034969) registry monitors the safety and effectiveness of icatibant for treating acute angioedema. Objective: Present findings
Anais Brasileiros de Dermatologia. Publicado em: 2022
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2. Hereditary angioedema: a disease seldom diagnosed by pediatricians
Abstract Objectives: To describe the hereditary angioedema to improve awareness of this condition and reduce diagnostic delay. Data sources: Relevant articles in the MEDLINE database through PubMed. Data synthesis: Hereditary angioedema is rare and has an autosomal dominant pattern of inheritance. Its onset occurs mainly in childhood, but there is an impo
J. Pediatr. (Rio J.). Publicado em: 2021-04
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3. Study of angiopoietin and plasminogen genes in hereditary angioedema
RESUMO OBJETIVO Investigar a presença das mutações no gene Angiopoietina (ANGPT1) e gene Plasminogênio (PLG) em pacientes com Angioedema Hereditário (AEH) com inibidor C1 esterase (C1-INH) normal e negativos para mutação do gene F12. MÉTODOS Foram avaliados pacientes com diagnóstico clínico de AEH sem deficiência ou disfunção de C1-INH e neg
Rev. Assoc. Med. Bras.. Publicado em: 2020-04
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4. Postoperative angioedema induced by angiotensin-converting enzyme inhibitor: case report
Resumo Justificativa e objetivos: O angioedema é uma condição potencialmente fatal que pode surgir em qualquer momento no perioperatório. Pode decorrer da liberação de histamina, em uma reação de hipersensibilidade a drogas ou ser desencadeado pela bradicinina, em reações não alérgicas, de etiologia hereditária ou adquirida. O objetivo desse re
Rev. Bras. Anestesiol.. Publicado em: 20/12/2019
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5. Hereditary angioedema with C1 inhibitor (C1-INH) deficit: the strength of recognition (51 cases)
Hereditary angioedema (HAE) is a rare autosomal dominant disease due to C1 esterase inhibitor deficiency (C1-INH). The disease is characterized by subcutaneous and submucosal edema in the absence of urticaria due to the accumulation of bradykinin. This descriptive study aimed to evaluate the clinical characteristics of patients with a confirmed diagnosis of
Braz J Med Biol Res. Publicado em: 14/11/2018
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6. Improving the Management of Hereditary Angioedema
Clinics. Publicado em: 17/05/2018
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7. Brazilian Guidelines for Hereditary Angioedema Management - 2017 Update Part 1: Definition, Classification and Diagnosis
Hereditary angioedema is an autosomal dominant disease characterized by recurrent angioedema attacks with the involvement of multiple organs. The disease is unknown to many health professionals and is therefore underdiagnosed. Patients who are not adequately diagnosed and treated have an estimated mortality rate ranging from 25% to 40% due to asphyxiation by
Clinics. Publicado em: 03/05/2018
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8. Outcomes of long term treatments of type I hereditary angioedema in a Turkish family
Abstract: Background: Hereditary angioedema is a rare autosomal dominantly inherited immunodeficiency disorder characterized by potentially life-threatening angioedema attacks. Objective: We aimed to investigate the clinical and genetic features of a family with angioedema attacks. Methods: The medical history, clinical features and C1-INH gene mutation o
An. Bras. Dermatol.. Publicado em: 2017-10
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9. Hereditary angioedema: quality of life in Brazilian patients
OBJECTIVE: Hereditary angioedema is a serious medical condition caused by a rare autosomal dominant genetic disorder and it is associated with deficient production or dysfunction of the C1 esterase inhibitor. In most cases, affected patients experience unexpected and recurrent crises of subcutaneous, gastrointestinal and laryngeal edema. The unpredictability
Clinics. Publicado em: 2013-01
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10. Avaliação da qualidade de vida de pacientes com angioedema hereditário / Quality of life assessment in patients with hereditary angioedema
INTRODUÇÃO: O angioedema hereditário (AEH) é uma doença rara, causada pela deficiência do inibidor de C1 esterase (C1-INH), que se manifesta por ataques recorrentes e imprevisíveis de edema em face, extremidades, genitais, tronco e trato gastrintestinal. O edema em vias superiores pode levar a asfixia e morte; enquanto que as crises de dor abdominal p
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 09/08/2011
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11. Avaliação do efeito de contraceptivos hormonais sobre o sistema complemento / Evaluation of the effect of hormonal contraceptives on the complement system
The occurrence of thrombosis is often associated with the presence of one or more risk factors, which may be genetic and/or acquired, such as hormonal changes that occur during pregnancy, hormone replacement therapy and the use of combined hormonal contraceptives (CHC). The inflammation in turn, is an important body\ s response to the aggression and involves
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 29/04/2011
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12. Brazilian guidelines for the diagnosis and treatment of hereditary angioedema
Hereditary angioedema is an autosomal dominant disease characterized by edema attacks with multiple organ involvement. It is caused by a quantitative or functional deficiency of the C1 inhibitor, which is a member of the serine protease inhibitor family. Hereditary angioedema is unknown to many health professionals and is therefore an underdiagnosed disease.
Clinics. Publicado em: 2011