Managing Diagnosis, Treatment, and Burden of Disease in Hereditary Angioedema Patients with Normal C1-Esterase Inhibitor
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DOI: 10.2147/jaa.s398333
Abstract: Abstract Hereditary angioedema (HAE) is a rare, chronic, and debilitating genetic disorder characterized by recurrent and unpredictable swelling episodes that primarily affect the subcutaneous and/or submucosal tissues of the extremities, larynx, face, abdomen, and genitals.… read more here.
Keywords: hae; hereditary angioedema; hae inh; diagnosis ... See more keywords