Impaired control of the contact system in hereditary angioedema with normal C1‐inhibitor,Allergy

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Impaired control of the contact system in hereditary angioedema with normal C1‐inhibitor
Allergy ( IF 12.6 ) Pub Date : 2020-02-06 , DOI: 10.1111/all.14160
Maria Bova ₁ , Chiara Suffritti ₂ , Valeria Bafunno ₃ , Stefania Loffredo _{1,

4} , Giorgia Cordisco ₃ , Stefano Del Giacco ₅ , Tiziana Maria Angela De Pasquale ₆ , Davide Firinu ₅ , Maurizio Margaglione ₃ , Vincenzo Montinaro ₇ , Angelica Petraroli ₁ , Anna Radice ₈ , Luisa Brussino ₉ , Andrea Zanichelli ₁₀ , Alessandra Zoli ₁₁ , Marco Cicardi _{2,

12}

Affiliation

Department of Translational Medical Sciences and Center for Basic and Clinical Immunology Research, University of Naples Federico II, Naples, Italy.
Department of Biomedical and Clinical Sciences Luigi Sacco, University of Milan, Milan, Italy.
Medical Genetics, Department of Clinical and Experimental Medicine, University of Foggia, Foggia, Italy.
Institute of Experimental Endocrinology and Oncology "G. Salvatore", National Research Council, Naples, Italy.
Department of Medical Sciences, University of Cagliari, Cagliari, Italy.
Civitanova Marche Hospital, Civitanova Marche, Italy.
Division of Nephrology, University of Bari, Bari, Italy.
Department of Allergy, University of Florence, Florence, Italy.
Department of Medical Science, University of Torino, Turin, Italy.
ASST Fatebenefratelli Sacco, Milano, Italy.
Department of Clinical Immunology, Ospedali Riuniti, Ancona, Italy.
IRCCS-ICS Maugeri, Milano, Italy.

Hereditary angioedema (HAE) comprises HAE with C1‐inhibitor deficiency (C1‐INH‐HAE) and HAE with normal C1‐INH activity (nl‐C1‐INH‐HAE), due to mutations in factor XII (FXII‐HAE), plasminogen (PLG‐HAE), angiopoietin 1 (ANGPT1‐HAE), kininogen 1 genes (KNG1‐HAE), or angioedema of unknown origin (U‐HAE). The Italian network for C1‐INH‐HAE (ITACA) created a registry including different forms of angioedema without wheals.

中文翻译：

C1抑制剂正常的遗传性血管性水肿中接触系统的控制受损

遗传性血管性水肿 (HAE) 包括 C1-抑制剂缺乏 (C1-INH-HAE) 和 C1-INH 活性正常的 HAE (nl-C1-INH-HAE)，这是由于因子 XII (FXII-HAE)、纤溶酶原的突变(PLG-HAE)、血管生成素 1 (ANGPT1-HAE)、激肽原 1 基因 (KNG1-HAE) 或来源不明的血管性水肿 (U-HAE)。意大利 C1-INH-HAE 网络 (ITACA) 创建了一个登记表，包括不同形式的无风团的血管性水肿。

更新日期：2020-02-06

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