{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,2,21]],"date-time":"2025-02-21T08:27:40Z","timestamp":1740126460073,"version":"3.37.3"},"reference-count":6,"publisher":"Oxford University Press (OUP)","issue":"10","license":[{"start":{"date-parts":[[2024,4,25]],"date-time":"2024-04-25T00:00:00Z","timestamp":1714003200000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/academic.oup.com\/pages\/standard-publication-reuse-rights"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2024,9,18]]},"abstract":"<jats:p>The identification of primary immunodeficiencies is often delayed because of the inherent clinical heterogeneity and gaps in clinicians\u2019 understanding of the clinical landscape. We present an unusual case of a patient with X-linked immunodeficiency with magnesium defect, Epstein\u2013Barr virus infection and neoplasia (XMEN) disease. 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