{Reference Type}: Case Reports
{Title}: Navigating the swells: A case report of hereditary angioedema.
{Author}: Taori K;Kirnake V;Junare P;Padwale V;
{Journal}: J Family Med Prim Care
{Volume}: 13
{Issue}: 7
{Year}: 2024 Jul
暂无{DOI}: 10.4103/jfmpc.jfmpc_1254_23
{Abstract}: Hereditary angioedema (HAE) is a rare genetic disorder characterized by recurrent episodes of localized edema caused by a deficiency or dysfunction of C1 inhibitor (C1-INH). This case report presents the clinical features, diagnostic evaluation, and management of a 23-year-old man with HAE. We discuss the challenges of diagnosing and treating this condition, emphasizing the importance of early recognition and appropriate therapeutic interventions.