Genetic Analysis As a Practical Tool to Diagnose Hereditary Angioedema with Normal C1 Inhibitor: A Case Report

Genetic Analysis As a Practical Tool to Diagnose Hereditary Angioedema with Normal C1 Inhibitor: A Case Report

Results During attacks, serum amylase and lipase were normal, with elevated white cell counts (13.970/mm3, 91% neutrophils) and C-reactive protein, without eosinophilia.

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Veröffentlicht in:Journal of allergy and clinical immunology 2015-02, Vol.135 (2), p.AB197-AB197
Hauptverfasser: Arruda, Luisa Karla P., MD, PhD, FAAAAI, Delcaro, Luana, BSc, Botelho Palhas, Priscila B., MD, Dias, Marina M., Chem, Muglia, Valdair F., MD, PhD, Castelli, Erick C., PhD, Bork, Konrad, MD, Moreno, Adriana S., PhD
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Sprache:eng
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Abdomen
Allergy and Immunology
Drug therapy
Mutation
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container_end_page AB197
container_issue 2
container_start_page AB197
container_title Journal of allergy and clinical immunology
container_volume 135
creator Arruda, Luisa Karla P., MD, PhD, FAAAAI
Delcaro, Luana, BSc
Botelho Palhas, Priscila B., MD
Dias, Marina M., Chem
Muglia, Valdair F., MD, PhD
Castelli, Erick C., PhD
Bork, Konrad, MD
Moreno, Adriana S., PhD
description Results During attacks, serum amylase and lipase were normal, with elevated white cell counts (13.970/mm3, 91% neutrophils) and C-reactive protein, without eosinophilia.
doi_str_mv 10.1016/j.jaci.2014.12.1578
format Article
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source Elsevier ScienceDirect Journals Complete; EZB-FREE-00999 freely available EZB journals
subjects Abdomen
Allergy and Immunology
Drug therapy
Mutation
title Genetic Analysis As a Practical Tool to Diagnose Hereditary Angioedema with Normal C1 Inhibitor: A Case Report
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