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Prematta, M., Gibbs, J.G., Pratt, E.L., Stoughton, T.R. and Craig, T.J. (2007) Fresh frozen plasma for the treatment of hereditary angioedema. Annals of Allergy, Asthma & Immunology, 98, 383-388. doi:10.1016/S1081-1206(10)60886-1

has been cited by the following article:

• TITLE: A C1-inhibitor rare mutation: Early diagnosis of hereditary angioedema in a paediatric patient

  AUTHORS: Maria Cristina Maggio, Piero Sammarco, Carmelo Fabiano, Giovanni Corsello

  KEYWORDS: Hereditary Angioedema; C1-Inhibitor Deficiency

  JOURNAL NAME: Open Journal of Pediatrics, Vol.3 No.1, March 21, 2013

  ABSTRACT: Hereditary angioedema secondary to C1-inhibitor deficiency is a rare autosomal dominant disorder characterized by a deficiency of C1 esterase inhibitor.An eight-year-old girl showed periorbital painless swelling, diagnosed as ethmoiditis. A craniofacial scan did not evidence a paranasal sinus involvement, C1INH levels were undetectable, with low C4 levels: 7.6 mg/dl and C1INH: