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GATA2 deficiency is an autosomal dominant, pleiotropic disease with clinical manifestations that include bone marrow failure, monocyte and B cell deficiency, leukemia, pulmonary alveolar proteinosis and lymphedema. We present the case of an infant identified by newborn screening for SCID due to GATA2 deficiency.<\/jats:p>","DOI":"10.3389\/fped.2022.1031106","type":"journal-article","created":{"date-parts":[[2023,1,16]],"date-time":"2023-01-16T04:45:00Z","timestamp":1673844300000},"update-policy":"https:\/\/doi.org\/10.3389\/crossmark-policy","source":"Crossref","is-referenced-by-count":1,"title":["GATA2 deficiency detected by newborn screening for SCID: A case report"],"prefix":"10.3389","volume":"10","author":[{"given":"Alejandra","family":"Escobar 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