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Topics:
Allergy & Immunology
•
Urticaria/Angioedema
Is there a role for genetic testing after diagnosing HAE?
Related Questions
Would you still consider omalizumab for CSU with angioedema in a patient with Factor V Leiden deficiency?
What is your experience managing patients with chronic spontaneous urticaria occurring only at night?
How do you approach performing a food challenge in a patient with CSU who is dependent on their H1 blockers?
What is your preferred prophylactic agent in idiopathic angioedema?
What medications do you counsel patients to avoid if they develop ACEi angioedema?
Can Xolair (omalizumab) be safely used in combination with biologics for patients with rheumatic disease?
How do you reassure families that no allergy testing is needed for urticaria?
Is there a role for phenotyping patients with CSU outside of a research setting by ordering IgG-anti-TPO, IgG-anti-FceRI , total IgE, total IgA etc.?
How often do you rely on using the C1 inhibitor functional assay versus the quantitative level alone to diagnose HAE?
Do you start omalizumab in childbearing patients with CSU?