A Case Report of Hereditary Angioedema: Challenges in Diagnosis and Management
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 whic...
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Interna Publishing,
2023-04-01T00:00:00Z.
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001 | doaj_8e07e868b8034ef8b16df5789a5a61f5 | ||
042 | |a dc | ||
100 | 1 | 0 | |a Alvina Widhani |e author |
700 | 1 | 0 | |a Suzy Maria |e author |
700 | 1 | 0 | |a Rifky Yulian |e author |
700 | 1 | 0 | |a Anshari Saifuddin Hasibuan |e author |
700 | 1 | 0 | |a Sukamto Koesnoe |e author |
245 | 0 | 0 | |a A Case Report of Hereditary Angioedema: Challenges in Diagnosis and Management |
260 | |b Interna Publishing, |c 2023-04-01T00:00:00Z. | ||
500 | |a 0125-9326 | ||
500 | |a 2338-2732 | ||
520 | |a 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. | ||
546 | |a EN | ||
690 | |a hereditary | ||
690 | |a angioedema | ||
690 | |a diagnosis | ||
690 | |a management | ||
690 | |a Internal medicine | ||
690 | |a RC31-1245 | ||
655 | 7 | |a article |2 local | |
786 | 0 | |n Acta Medica Indonesiana, Vol 55, Iss 2 (2023) | |
787 | 0 | |n https://actamedindones.org/index.php/ijim/article/view/2217 | |
787 | 0 | |n https://doaj.org/toc/0125-9326 | |
787 | 0 | |n https://doaj.org/toc/2338-2732 | |
856 | 4 | 1 | |u https://doaj.org/article/8e07e868b8034ef8b16df5789a5a61f5 |z Connect to this object online. |