Angioedemas, hereditary - Open Access .click

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Analysis of Sleep Quality in Patients with Hereditary Angioedema

ABCS Health Sciences
Introduction: Sleep plays a crucial role in human health, both physiologically and mentally, responsible for body repair and regeneration. This may be affected by patients with Hereditary Angioedema (HAE), a rare and serious genetic disease of the ...
Tatielly Kruk +8 more
doaj +1 more source

Art v 1 and Amb a 4 Co‐Sensitization Identifies Italian Patients at Risk for Mugwort‐Celery‐Spice Syndrome

Allergy, EarlyView.
Three molecular profiles identified among Art v 1/Amb a 4‐sensitized patients: Art v 1 monosensitization, Amb a 4 monosensitization, and dual sensitization to both allergens. Art v 1 monosensitization was predominantly associated with allergic rhinitis, reflecting a classical airborne allergy pattern.
Enrico Scala +20 more
wiley +1 more source

Unmet Needs in Treatment Escalation for Chronic Spontaneous Urticaria: Findings From the CURE Registry

Allergy, EarlyView.
Appropriate treatment escalation improves CSU disease control. However, only about a quarter of patients achieve a complete response, the main goal of CSU treatment. Approximately one‐third of patients clinically eligible for escalation (UCT < 12) do not receive guideline‐recommended treatment escalation and remain symptomatic on their current ...
Pavel Kolkhir +25 more
wiley +1 more source

Unmet needs in the management of hereditary angioedema from the perspective of Brazilian patients

World Allergy Organization Journal
Introduction: Hereditary angioedema (HAE) is a rare genetic disease characterized by recurrent, potentially life-threatening angioedema episodes. Despite its severity, including the risk of asphyxiation, HAE often remains underdiagnosed.
Pedro Giavina-Bianchi, MD, PhD +4 more
doaj +1 more source

Características clínicas y sociodemográficas de la población con diagnóstico de angioedema, atendida en un centro de referencia en Medellín, Colombia; periodo 2013-2018 [PDF]

, 2021
RESUMEN Antecedentes: el angioedema comprendido como enfermedad mas no como síntoma, tiene unas características particulares y unos subtipos definidos. En Colombia no hay descripciones de las características clínicas y sociodemográficas de los pacientes ...
Fuentes Abreu, Fernando Estiven, Sosa Moreno, Jaime Andrés +1 more
core

International Guideline on the Diagnosis and Management of Pediatric Patients With Hereditary Angioedema

Allergy, EarlyView.
ABSTRACT Hereditary angioedema (HAE) with C1 inhibitor deficiency is a rare disease characterized by unpredictable episodes of tissue swelling (angioedema), which, in most cases, occur first under the age of 18 years, and entail a significant burden of disease not only for the patients but also for their families.
Henriette Farkas +128 more
wiley +1 more source

ID280 MHT para profilaxia de crises de AEH tipo I e II para maiores de 2 anos de idade, gestantes ou lactantes

Jornal de Assistência Farmacêutica e Farmacoeconomia
Introdução O angioedema hereditário (AEH) por deficiência de C1-esterase é uma doença genética rara caracterizada pela deficiência ou disfunção do inibidor do C1-INH, também denominada tipo I ou tipo II.
Aramís Tupiná Alcântara de Moreira +3 more
doaj +1 more source

The International Guideline for the Definition, Classification, Diagnosis and Management of Urticaria

Allergy, EarlyView.
ABSTRACT This update and revision of the international guideline for urticaria was developed in accordance with the methods recommended by Cochrane and the Grading of Recommendations Assessment, Development and Evaluation (GRADE) working group. It is an initiative of the Global Allergy and Asthma Excellence Network (GA2LEN) and its Urticaria and ...
T. Zuberbier +221 more
wiley +1 more source

ID279 MHT para tratamento de crises de AEH para maiores de 2 anos de idade

Jornal de Assistência Farmacêutica e Farmacoeconomia
Introdução O angioedema hereditário (AEH) por deficiência de C1-esterase é uma doença genética rara caracterizada pela deficiência ou disfunção do inibidor do C1-INH.
Aramís Tupiná Alcântara de Moreira +4 more
doaj +1 more source

Development of Betalactam‐Predictor: A Clinical Decision Tool for Delabeling Low‐Risk Betalactam Allergy Patients. Initial Validation in Penicillin Allergy

Allergy, EarlyView.
BL‐Predictor has emerged as a new tool for delabeling penicillin allergy. External validation has shown a specificity of 93% for detecting low‐risk patients. This score could potentially reduce diagnostic costs and the negative consequences associated with incorrect antibiotic allergy labels.
Marina Labella +14 more
wiley +1 more source

angioedema
3. good health
complement c1 inactivator proteins

complement c1 inhibitor protein
female
angioedemas

adult
hereditary
bradykinin