Reliable information

References and guidelines

Institutional sources, associations and official documents on Hereditary Angioedema (HAE).

Abranghe Community

Patients, family members and healthcare professionals can follow Abranghe's official channels to receive information, announcements and educational materials.

Instagram

Informational content, announcements and outreach materials.

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Facebook

Institutional page for communication and outreach.

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Facebook Group

Support group for patients and families to share experiences.

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Social media channels do not replace medical follow-up or treatment.

Important links

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 may also help patients and families understand the recommended clinical 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 website

Source: Ministry of Health — Brazilian Federal Government.