Clinical Phenotypes and Immunological Characteristics of 18 Egyptian LRBA Deficiency Patients
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DOI: 10.1007/s10875-020-00799-2
Abstract: LPS-responsive beige-like anchor (LRBA) deficiency is an autosomal recessive primary immunodeficiency disorder, OMIM (#614700). LRBA deficiency patients suffer from variable manifestations including recurrent infections, immune dysregulation, autoimmunity, cytopenias, and enteropathy. This study describes different clinical… read more here.
Keywords: deficiency patients; phenotypes immunological; immunological characteristics; clinical phenotypes ... See more keywords