Spectrum of diagnosis of hereditary angioedema: Seven case reports

Spectrum of diagnosis of hereditary angioedema: Seven case reports

Hereditary angioedema (HAE) is a potentially life-threatening disorder, due to a mutation in complement one-inhibitor (C1-INH) gene, which blocks the activity of various components of complement – fibrinolytic and bradykinin control system. Our seven cases of HAE give different clinical presentation...

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Bibliographic Details
Main Authors: P C Kathuria, Manisha Rai, Neelam Kathuria
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2020-01-01
Series:Indian Journal of Allergy Asthma and Immunology
Subjects:
c1-inhibitor
c3
c4
fresh frozen plasma
hereditary angioedema
hypothalamus–pituitary–adrenal axis suppression
Online Access:http://www.ijaai.in/article.asp?issn=0972-6691;year=2020;volume=34;issue=1;spage=49;epage=52;aulast=Kathuria

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http://www.ijaai.in/article.asp?issn=0972-6691;year=2020;volume=34;issue=1;spage=49;epage=52;aulast=Kathuria

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