Complement Study Versus CINH Gene Testing for the Diagnosis of Type I Hereditary Angioedema in Children

Overview

Journal J Clin Immunol

Publisher Springer

Specialty Allergy & Immunology

Date 2015 Dec 15

PMID 26661330

Citations 10

Authors

Maria Pedrosa

Elsa Phillips-Angles

Alberto Lopez-Lera

Margarita Lopez-Trascasa

Teresa Caballero

Affiliations

Soon will be listed here.

Citing Articles

Characteristics and Drug Utilization of Patients with Hereditary Angioedema in Italy, a Real-World Analysis.

Giacomini E, Leogrande M, Perrone V, Andretta M, Bacca M, Chinellato A Healthcare (Basel). 2023; 11(18).

PMID: 37761706 PMC: 10530529. DOI: 10.3390/healthcare11182509.

The impact of puberty on the onset, frequency, location, and severity of attacks in hereditary angioedema due to C1-inhibitor deficiency: A survey from the Italian Network for Hereditary and Acquired Angioedema (ITACA).

Cancian M, Triggianese P, Modica S, Arcoleo F, Bignardi D, Brussino L Front Pediatr. 2023; 11:1141073.

PMID: 37144145 PMC: 10152551. DOI: 10.3389/fped.2023.1141073.

Pediatric Angioedema without Wheals: How to Guide the Diagnosis.

Liotti L, Pecoraro L, Mastrorilli C, Castagnoli R, Saretta F, Mori F Life (Basel). 2023; 13(4).

PMID: 37109550 PMC: 10141554. DOI: 10.3390/life13041021.

Diagnosing Pediatric Patients With Hereditary C1-Inhibitor Deficiency-Experience From the Hungarian Angioedema Center of Reference and Excellence.

Andrasi N, Balla Z, Visy B, Szilagyi A, Csuka D, Varga L Front Allergy. 2022; 3:860355.

PMID: 35769571 PMC: 9234934. DOI: 10.3389/falgy.2022.860355.

The international WAO/EAACI guideline for the management of hereditary angioedema - The 2021 revision and update.

Maurer M, Magerl M, Betschel S, Aberer W, Ansotegui I, Aygoren-Pursun E World Allergy Organ J. 2022; 15(3):100627.

PMID: 35497649 PMC: 9023902. DOI: 10.1016/j.waojou.2022.100627.

References

Roche O, Blanch A, Duponchel C, Fontan G, Tosi M, Lopez-Trascasa M . Hereditary angioedema: the mutation spectrum of SERPING1/C1NH in a large Spanish cohort. Hum Mutat. 2005; 26(2):135-44. DOI: 10.1002/humu.20197. View

Caballero T, Baeza M, Cabanas R, Campos A, Cimbollek S, Gomez-Traseira C . Consensus statement on the diagnosis, management, and treatment of angioedema mediated by bradykinin. Part I. Classification, epidemiology, pathophysiology, genetics, clinical symptoms, and diagnosis. J Investig Allergol Clin Immunol. 2011; 21(5):333-47. View

Nielsen E, Johansen H, Holt J, Mollnes T . C1 inhibitor and diagnosis of hereditary angioedema in newborns. Pediatr Res. 1994; 35(2):184-7. DOI: 10.1203/00006450-199402000-00012. View

Lopez-Lera A, Garrido S, Roche O, Lopez-Trascasa M . SERPING1 mutations in 59 families with hereditary angioedema. Mol Immunol. 2011; 49(1-2):18-27. DOI: 10.1016/j.molimm.2011.07.010. View

Craig T, Aygoren-Pursun E, Bork K, Bowen T, Boysen H, Farkas H . WAO Guideline for the Management of Hereditary Angioedema. World Allergy Organ J. 2013; 5(12):182-99. PMC: 3651186. DOI: 10.1097/WOX.0b013e318279affa. View