Navigating the swells: A case report of hereditary angioedema

Autor:	Kamlesh Taori, Vijendra Kirnake, Parmeshwar Junare, Vishal Padwale
Jazyk:	angličtina
Rok vydání:	2024
Předmět:	c1 inhibitor deficiency hereditary angioedema recurrent angioedema Medicine
Zdroj:	Journal of Family Medicine and Primary Care, Vol 13, Iss 7, Pp 2784-2786 (2024)
Druh dokumentu:	article
ISSN:	2249-4863 2278-7135
DOI:	10.4103/jfmpc.jfmpc_1254_23
Popis:	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.
Databáze:	Directory of Open Access Journals
Externí odkaz:	https://doaj.org/article/bd94b269b3854fc08cd977f30ec336e8 Zobrazit plný text záznamu View record in DOAJ Plný text ve formátu PDF