Chronic Granulomatous Disease with the McLeod Phenotype: a French National Retrospective Case Series

ConclusionThis is the largest yet descriptive study of a series of patients with X-linked CGD and the McLeod phenotype. Although this disease combination is rare, the timely, accurate diagnosis of the McLeod phenotype is critical because of the serious post-transfusion complications. However, HSCT can be considered in these patients.

http://link.springer.com/10.1007/s10875-020-00791-w

Source: Journal of Clinical Immunology - June 18, 2020 Category: Allergy & Immunology Source Type: research