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549 Management of Twenty-Five Pediatric Patients with Hereditary Angioedema (Hae) Undergoing Home Treatment—A Clinical Surveillance Program

BACKGROUND: Hereditary angioedema (HAE) is a rare disorder characterized by C1 esterase inhibitor (C1-INH) deficiency. Clinically, HAE is characterized by relapsing episodes of edema at various body sites followed by disease-free intervals of variable duration. Episodes of upper airway obstruction (...

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Detalles Bibliográficos
Autores principales:	Martinez-Saguer, Inmaculada, Aygören-Pürsün, Emel, Rusicke, Eva, Klingebiel, Thomas, Kreuz, Wolfhart
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	World Allergy Organization Journal 2012
Materias:	Abstracts of the XXII World Allergy Congress
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3512583/ http://dx.doi.org/10.1097/01.WOX.0000411664.07634.b7

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