Doctor registration
If you treat HAE patients and would like to be included in Abranghe's network, please fill out the form below.
Registration submitted successfully!
Your information will be reviewed and added to the list shortly.
Could not confirm the submission.
Please try again or send your information to abranghe@gmail.com.
Virtual assistant
Information for healthcare professionals
Chat with our virtual assistant for technical information about HAE diagnosis, treatment, clinical protocols, and therapeutic guidelines.
This assistant gathers articles and informational content about Hereditary Angioedema for educational purposes. If you'd like to contribute to our collection, you can send PDF files directly through the chat.
Brazilian HAE Guidelines
The Brazilian Hereditary Angioedema Guidelines (2022) compile updated recommendations for diagnosis, classification, and treatment of the disease, based on scientific evidence and consensus among Brazilian specialists.
The document is primarily aimed at healthcare professionals, but can also help patients and families understand the recommended practices in Brazil.
Source: Brazilian Association of Allergy and Immunology (ASBAI).
PCDT — Clinical Protocol and Therapeutic Guidelines
The PCDT for Angioedema due to C1-Esterase Deficiency (2016) is the official protocol from the Brazilian Ministry of Health that establishes criteria for diagnosis, treatment, and follow-up through the public health system (SUS).
Access PCDT on the Ministry of Health websiteSource: Ministry of Health — Brazilian Federal Government.
Scientific reference
GEBRAEH
The Brazilian Study Group on Hereditary Angioedema brings together specialists, publishes guidelines, and maintains up-to-date resources about HAE.