A Case Report of Hereditary Angioedema: Challenges in Diagnosis and Management

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DC Field	Value	Language
dc.contributor.author	Widhani, Alvina	-
dc.contributor.author	Maria, Suzy	-
dc.contributor.author	Yulian, Rifky	-
dc.contributor.author	Saifuddin Hasibuan, Anshari	-
dc.contributor.author	Koesnoe, Sukamto	-
dc.date.accessioned	2024-12-14T03:08:30Z	-
dc.date.available	2024-12-14T03:08:30Z	-
dc.date.issued	2023-04-02	-
dc.identifier.issn	2338-2732	-
dc.identifier.uri	http://localhost:8080/xmlui/handle/123456789/8968	-
dc.description.abstract	ABSTRACT Hereditary angioedema (HAE) is a rare autosomal dominant genetic disorder which causes bradykinin mediated angioedema. Although it can be life threatening, HAE may be underdiagnosed due to a lack of awareness of the disease and limited access to laboratory testing. Here, we report a case of HAE which was diagnosed only after the patient was referred for COVID-19 vaccination even though he had been experiencing recurrent angioedema for the past 30 years. Keywords: Hereditary, angioedema, diagnosis, management.	en_US
dc.language.iso	en	en_US
dc.publisher	Perhimpunan Dokter Spesialis Penyakit dalam Indonesia	en_US
dc.subject	Hereditary,	en_US
dc.subject	angioedema,	en_US
dc.subject	diagnosis,	en_US
dc.subject	management.	en_US
dc.title	A Case Report of Hereditary Angioedema: Challenges in Diagnosis and Management	en_US
dc.type	Article	en_US
Appears in Collections:	VOL 55 NO 2 2023

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