Department of Health, Motherhood and Childhood Advancement Sciences, University of Palermo, Palermo, Italy
Operative Unit of Molecular Genetic Laboratory, Ospedali Riuniti Villa Sofia-Cervello, Palermo, Italy
Operative Unit of Molecular Genetic Laboratory, Ospedali Riuniti Villa Sofia-Cervello, Palermo, Italy
Department of Health, Motherhood and Childhood Advancement Sciences, University of Palermo, Palermo, Italy
Copyright © 2013 Maria Cristina Maggio, Piero Sammarco, Carmelo Fabiano, Giovanni Corsello et al. This is
an open access article distributed under the Creative Commons Attribution
License, which permits unrestricted use, distribution, and reproduction in any
medium, provided the original work is properly cited.
How to Cite this Article
Maggio, M. , Sammarco, P. , Fabiano, C. and Corsello, G. (2013) A C1-inhibitor rare mutation: Early diagnosis of hereditary angioedema in a paediatric patient.
Open Journal of Pediatrics,
3, 42-44. doi:
10.4236/ojped.2013.31008.