Common variable immune deficiency with mutated TNFSRF13B gene presenting with autoimmune hematologic manifestations

Common variable immune deficiency with mutated TNFSRF13B gene presenting with autoimmune hematologic manifestations

Patients with common variable immunodeficiency (CVID) develop autoimmune hematologic manifestations. We report a 14-year-old boy with Evans syndrome, who presented at the age of 11.5 years with autoimmune hemolysis and was successfully managed with corticosteroids. Initially, the serum immunoglobuli...

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Bibliographic Details
Main Authors: Elpis Mantadakis, Evangelia Farmaki, Anna Taparkou, Athanassios Chatzimichael, Matthaios Speletas
Format: Article
Language:English
Published: Elsevier 2016-10-01
Series:Pediatric Hematology Oncology Journal
Subjects:
Common variable immune deficiency
Autoimmune hemolytic anemia
Immune thrombocytopenia
Transmembrane activator and CAML interactor
Online Access:http://www.sciencedirect.com/science/article/pii/S2468124516301826

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http://www.sciencedirect.com/science/article/pii/S2468124516301826

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