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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.
Journal of Clinical Immunology
|September 29, 2017
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.
Area of Science:
- Immunology
- Genetics
- Pediatrics
Background:
- LPS-responsive beige-like anchor protein (LRBA) deficiency is a primary immunodeficiency.
- It is often associated with common variable immunodeficiency, autoimmunity, and inflammatory bowel diseases.
- The clinical spectrum of LRBA deficiency is broader than previously recognized.
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