Reply to “A Case Report about the Management of Hereditary Angioedema with Normal Complement Levels during Pregnancy”
DOI:
https://doi.org/10.20344/amp.20458Keywords:
Angioedemas, Hereditary/complications, Complement C1 Inactivator Proteins, Pregnancy ComplicationsAbstract
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Pinto AR, Machado Cunha I, Carolino F. A case report about the management of hereditary angioedema with normal complement levels during pregnancy. Acta Med Port. 2023;36:453-4. DOI: https://doi.org/10.20344/amp.19620
Cosme J, Spínola A, Ferreira MB, Barbosa MP. Hospitalizations due to angioedema without urticaria in a Portuguese center: five year retrospective study. Acta Med Port. 2019;32:714-20. DOI: https://doi.org/10.20344/amp.11893
Gabriel N, Marcelino F, Ferriani MP, Arruda LK, Campos RA, Gonçalves RF, et al. Pregnancy in patients with hereditary angioedema and normal C1 inhibitor. Front Allergy. 2022;17;3:846968. DOI: https://doi.org/10.3389/falgy.2022.846968
Varandas C, Esteves Caldeira L, Silva SL, Costa C, Limão R, Silva MI, et al. Hereditary angioedema: 24 years of experience in a Portuguese reference center. Eur Ann Allergy Clin Immunol. 2022 (in press). doi: 10.23822/EurAnnACI.1764-1489.278. DOI: https://doi.org/10.23822/EurAnnACI.1764-1489.278
Caballero T, Farkas H, Bouillet L, Bowen T, Gompel A, Fagerberg C, et al. International consensus and practical guidelines on the gynecologic and obstetric management of female patients with hereditary angioedema caused by C1 inhibitor deficiency. J Allergy Clin Immunol. 2012;129:308-20. DOI: https://doi.org/10.1016/j.jaci.2011.11.025
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