Delayed diagnosis of hereditary angioedema with C1-inhibitor deficiency in iranian children and adolescents

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

Research output: Contribution to journalLetter

Original languageEnglish
Pages (from-to)395-398
Number of pages4
JournalPediatric Allergy and Immunology
Volume30
Issue number3
DOIs
Publication statusPublished - May 2019

Keywords

  • Iran
  • adolescent
  • age of onset
  • child
  • complement C1 inhibitor protein
  • delayed diagnosis
  • hereditary angioedema types I and II
  • precipitating factors

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Immunology and Allergy
  • Immunology

Cite this

Ayazi, M., Fazlollahi, M. R., Mohammadzadeh, I., Fayezi, A., Nabavi, M., Mahdaviani, S. A., Movahedi, M., Heidarzadeh, M., Saghafi, S., Shokouhi Shoormasti, R., Mohammadian, S., Farkas, H., & Pourpak, Z. (2019). Delayed diagnosis of hereditary angioedema with C1-inhibitor deficiency in iranian children and adolescents. Pediatric Allergy and Immunology, 30(3), 395-398. https://doi.org/10.1111/pai.13028