{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,6]],"date-time":"2026-05-06T13:59:56Z","timestamp":1778075996473,"version":"3.51.4"},"reference-count":16,"publisher":"Wiley","issue":"5","license":[{"start":{"date-parts":[[2020,8,4]],"date-time":"2020-08-04T00:00:00Z","timestamp":1596499200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Pediatric Dermatology"],"published-print":{"date-parts":[[2020,9]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Rhizomelic chondrodysplasia punctata is a rare, often fatal disease that shares many clinical dysmorphologic features with the rare often non\u2010lethal chondrodysplasia punctata due to maternal autoimmune disease. Characteristic findings of both conditions include mid\u2010face hypoplasia, stippled epiphyses of the vertebrae and long bones, and growth failure. A growing association with anti\u2010ribonucleoprotein antibodies is emerging amongst patients with chondrodysplasia punctata due to maternal autoimmune disease and also neonatal lupus that have potential important screening implications. We present a unique case of chondrodysplasia punctata with neonatal lupus in the setting of positive anti\u2010RNP antibodies and negative anti\u2010Ro\/SSA and \u2013La\/SSB antibodies born to a mother with mixed connective tissue disease and Raynaud's syndrome.<\/jats:p>","DOI":"10.1111\/pde.14312","type":"journal-article","created":{"date-parts":[[2020,8,4]],"date-time":"2020-08-04T11:52:49Z","timestamp":1596541969000},"page":"925-928","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":2,"title":["Chondrodysplasia punctata and neonatal lupus in an infant with positive anti\u2010RNP and negative anti\u2010Ro\/SSA and \u2013La\/SSB antibodies, a case report"],"prefix":"10.1111","volume":"37","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-2116-8107","authenticated-orcid":false,"given":"Michael","family":"Milliken","sequence":"first","affiliation":[{"name":"Department of Dermatology University of Utah Salt Lake City UT USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jack","family":"Lee","sequence":"additional","affiliation":[{"name":"Department of Dermatology University of Virginia Charlottesville VA USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-0888-1458","authenticated-orcid":false,"given":"Sarah D.","family":"Cipriano","sequence":"additional","affiliation":[{"name":"Department of Dermatology University of Utah Salt Lake City UT USA"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2020,8,4]]},"reference":[{"key":"e_1_2_6_2_1","doi-asserted-by":"publisher","DOI":"10.1542\/peds.2006-2997"},{"key":"e_1_2_6_3_1","first-page":"487","article-title":"Severe rhizomelic chondrodysplasia punctata in a fetus due to maternal mixed connective tissue disorder","volume":"23","author":"Nayak SS","year":"2012","journal-title":"Genet 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