Refractory immune thrombocytopenia successfully treated with bortezomib in a child with 22q11.2 deletion syndrome, complicated by Evans syndrome and hypogammaglobulinemia-Reference-Cited by-同舟云学术

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Refractory immune thrombocytopenia successfully treated with bortezomib in a child with 22q11.2 deletion syndrome, complicated by Evans syndrome and hypogammaglobulinemia

Published:2022-02-08 Issue:5 Volume:33 Page:801-806
ISSN:0953-7104
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language:en
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Author:

Conti Francesca¹,Gottardi Francesca²^ORCID,Moratti Mattia²,Belotti Tamara¹,Ferrari Simona³,Selva Paola¹,Bassi Mirna⁴,Zama Daniele¹,Pession Andrea¹^ORCID

Affiliation:

1. Pediatric Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy

2. Specialty School of Paediatrics, University of Bologna, Bologna, Italy

3. Medical Genetics Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy

4. Laboratory of Immuno-haematology - Laboratorio Unico Metropolitano, Azienda USL, Bologna, Italy

Funder

funding

Publisher

Informa UK Limited

Subject

Hematology,General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/09537104.2021.2002835

Reference15 articles.

1. Pediatric Evans syndrome is associated with a high frequency of potentially damaging variants in immune genes

2. Refractory autoimmune cytopenias in pediatric Evans syndrome with underlying systemic immune dysregulation

3. Immune cytopenias as a continuum in inborn errors of immunity: An in‐depth clinical and immunological exploration

4. Immunophenotype Anomalies Predict the Development of Autoimmune Cytopenia in 22q11.2 Deletion Syndrome

5. How I manage Evans Syndrome and AIHA cases in children

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