A clinical overview of hereditary angioedema (HAE), including its pathophysiology, genetic subtypes, diagnosis, disease burden, and impact on quality of life.
Videos: Rare Takes
Johnathan A. Bernstein, MD, answers the most common and challenging questions surrounding HAE diagnosis and treatment complications. These short, focused Q&As provide practical strategies for managing real-world patient scenarios.
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In this Guide
A clinical overview of hereditary angioedema (HAE), including its pathophysiology, genetic subtypes, diagnosis, disease burden, and impact on quality of life.
Lab and genetic testing strategies to help diagnose HAE, including how to distinguish subtypes and evaluate patients with normal C1-INH levels.
Know what to expect from multisystem manifestations of HAE, including cutaneous, GI, upper airway, and other potentially life-threatening organ involvement.
A review of current and emerging long-term prophylactic therapies for HAE, including unique mechanisms, efficacy, and factors that guide treatment selection.
Inside the latest on-demand therapies for HAE, including unique mechanisms, efficacy, administration, and factors guiding treatment selection.
How to monitor HAE attacks, assess disease burden and treatment response, identify triggers, and optimize ongoing management and emergency preparedness.