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Mutations in the <jats:italic>SMARCAL1<\/jats:italic> gene (SW1\/SNF2\u2010related, matrix\u2010associated, actin\u2010dependent regulator of chromatin, subfamily a\u2010like1) cause SIOD. We report a patient with SIOD and SMARCAL1 mutations, who presented with fever of unknown origin secondary to B\u2010cell lymphoma. To our knowledge, this is the first report of an SIOD patient with a primary lymphoproliferative disorder (LPD). \u00a9 2004 Wiley\u2010Liss, Inc.<\/jats:p>","DOI":"10.1002\/ajmg.a.30356","type":"journal-article","created":{"date-parts":[[2004,11,12]],"date-time":"2004-11-12T23:50:19Z","timestamp":1100303419000},"page":"194-199","source":"Crossref","is-referenced-by-count":12,"title":["Fatal lymphoproliferative disorder in a child with Schimke immuno\u2010osseous dysplasia"],"prefix":"10.1002","volume":"131A","author":[{"given":"Doris","family":"Taha","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Cornelius F.","family":"Boerkoel","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"John 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