Multiple Presentations of LRBA Deficiency: a Single-Center Experience

Sevgi Kostel Bal1, Sule Haskologlu1, Nina K Serwas2,3

  • 1Department of Pediatric Allergy and Immunology, Ankara University School of Medicine, Cebeci, 06590, Ankara, Turkey.

Summary

LPS-responsive beige-like anchor protein (LRBA) deficiency presents diverse symptoms, including organomegaly and autoimmunity, not always hypogammaglobulinemia. Early hematopoietic stem cell transplantation (HSCT) offers a life-saving treatment for LRBA deficiency.

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