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Haapaniemi, E.M., Kaustio, M., Rajala, H.L.M., van Adrichem, A.J., Kainulainen, L., Glumoff, V., et al. (2015) Autoimmunity, Hypogammaglobulinemia, Lymphoproliferation, and Mycobacterial Disease in Patients with Activating Mutations in STAT3. Blood, 125, 639-648. https://doi.org/10.1182/blood-2014-04-570101

has been cited by the following article:

• TITLE: Phenocopies: Mimics of Inborn Errors of Immunity

  AUTHORS: Cesar Daniel Alonso-Bello, Sara Elva, Mariano Daniel Témix-Delfín, Fernando Lozano-Patiño, Victoria Isabel Castañeda-Avila, María Eugenia Vargas-Camaño, María Isabel Castrejón-Vázquez

  KEYWORDS: Phenocopies, Primary, Deficiency, Immunologic Deficiency Syndrome

  JOURNAL NAME: Open Access Library Journal, Vol.7 No.1, January 14, 2020

  ABSTRACT: A phenocopy is defined as a clinical non-inherited phenotype in an indi-vidual, with environmental induction, which is identical to the genetically determined phenotype of another. Until February 2017, the IUIS (Interna-tional Union of Immunological Societies) reported in its classification 354 innate immunity errors and a final group (classification table IX) with con-ditions that are not part of the innate alterations and are called phenocopies. These are classified into two types, the associated with somatic mutations and those associated with auto-antibodies. The phenotypes that occur by any of the mechanisms mentioned are complex and varied. It is necessary to know the clinical manifestations of the pathologies classified in this group to enrich the possible differential diagnoses in individuals with suspected immunodeficiency.