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We describe an adolescent with monosomy 7 CMML presenting as central diabetes insipidus (DI), who was treated with venetoclax and decitabine as a bridge to hematopoietic stem cell transplantation (HSCT). Central DI is a rare manifestation of monosomy 7\u2010associated MDS including CMML, itself a rare manifestation of GATA2 deficiency, particularly in children. Venetoclax\/decitabine was effective for treatment of CMML as a bridge to HSCT.<\/jats:p>","DOI":"10.1002\/pbc.28865","type":"journal-article","created":{"date-parts":[[2020,12,27]],"date-time":"2020-12-27T18:11:01Z","timestamp":1609092661000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":6,"title":["Venetoclax\/decitabine for a pediatric patient with chronic myelomonocytic leukemia"],"prefix":"10.1002","volume":"68","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-3142-516X","authenticated-orcid":false,"given":"John C.","family":"Molina","sequence":"first","affiliation":[{"name":"Pediatric Oncology Branch Center for Cancer Research (CCR) National Cancer Institute (NCI) NIH  Bethesda Maryland"},{"name":"Department of Pediatric Oncology Johns Hopkins Hospital  Baltimore Maryland"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Julie 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