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Start Over Descriptor "Hereditary angioedema types I and II" Region iran
1 results on '"Hereditary angioedema types I and II"'

1. Delayed diagnosis of hereditary angioedema with C1‐inhibitor deficiency in iranian children and adolescents.

Author

Ayazi, Maryam, Fazlollahi, Mohammad Reza, Mohammadzadeh, Iraj, Fayezi, Abbas, Nabavi, Mohammad, Mahdaviani, Seyed Alireza, Movahedi, Masoud, Heidarzadeh, Marzieh, Saghafi, Shiva, Shokouhi Shoormasti, Raheleh, Mohammadian, Sajedeh, Farkas, Henriette, and Pourpak, Zahra

Subjects
*ADOLESCENCE, *ANGIONEUROTIC edema, *CHILDREN, *COMPLEMENT inhibition
Abstract

The article offers a study that reveals Hereditary angioedema, an autosomal dominant deficiency of C1‐inhibitor (C1‐INH‐HAE). Topics discussed include disease that rises bradykinin‐mediated edema in face, trunk, extremities, and gastrointestinal tract; mentions the outcomes of Hereditary angioedema as asphyxiation, unnecessary emergency abdominal surgeries, and a considerably diminished quality of life; and information on establishing the screening program to optimize diagnosis.

Published
2019
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