{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,25]],"date-time":"2026-09-25T00:37:06Z","timestamp":1790296626727,"version":"4.1.0"},"reference-count":19,"publisher":"SAGE Publications","issue":"1","license":[{"start":{"date-parts":[[2024,9,26]],"date-time":"2024-09-26T00:00:00Z","timestamp":1727308800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["Pediatr Dev Pathol"],"published-print":{"date-parts":[[2025,1]]},"abstract":"<jats:p>Casamassima-Morton-Nance syndrome (CMNS) is a rare disorder characterized by spondylocostal dysostosis (SCD), anal atresia, and urogenital anomalies. We describe a fetus with CMNS associated with a limb-body wall defect (LBWD), the second such case in the literature. We compare the phenotypic differences with previously reported cases, including those with segmentation anomalies of the axial skeleton, body wall defects, or absent\/abnormal genitalia, revealing the consistent presence of SCD in CMNS. However, as expected, a wide phenotypic spectrum emerges, providing useful observations for fetal\/neonatal screening relevant to differential diagnoses. Advanced diagnostic methods using imaging and next-generation skeletal dysplasia multi-gene panels are advisable, as they enable timely, actionable, well-informed decisions for parental counseling, potential elective termination of pregnancy, and prenatal and\/or postnatal care. Most reported cases do not mention the recurrence of these usually lethal anomalies.<\/jats:p>","DOI":"10.1177\/10935266241281797","type":"journal-article","created":{"date-parts":[[2024,9,26]],"date-time":"2024-09-26T04:49:41Z","timestamp":1727326181000},"page":"63-67","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":2,"title":["Casamassima-Morton-Nance Syndrome and Limb-Body Wall Defect: Presentation of the Second Case and Phenotypic Assessment"],"prefix":"10.1177","volume":"28","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-4852-8026","authenticated-orcid":false,"given":"V\u00edctor M.","family":"Salinas-Torres","sequence":"first","affiliation":[{"name":"Secretaria de Salud Durango, Durango General Hospital, Human Genetics and Genomics Department, Durango, M\u00e9xico"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Rafael A.","family":"Salinas-Torres","sequence":"additional","affiliation":[{"name":"Instituto Tecnol\u00f3gico de Tijuana, Systems and Computing Department, Tijuana, Baja California, M\u00e9xico"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"179","published-online":{"date-parts":[[2024,9,26]]},"reference":[{"key":"bibr1-10935266241281797","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320080114"},{"key":"bibr2-10935266241281797","doi-asserted-by":"publisher","DOI":"10.2350\/15-08-1682-CR.1"},{"key":"bibr3-10935266241281797","doi-asserted-by":"publisher","DOI":"10.1136\/jmg.25.5.340"},{"key":"bibr4-10935266241281797","doi-asserted-by":"publisher","DOI":"10.1016\/S0344-0338(00)80114-4"},{"key":"bibr5-10935266241281797","doi-asserted-by":"publisher","DOI":"10.1016\/j.ejmg.2006.08.001"},{"key":"bibr6-10935266241281797","doi-asserted-by":"publisher","DOI":"10.3109\/15513815.2015.1055021"},{"key":"bibr7-10935266241281797","doi-asserted-by":"publisher","DOI":"10.1055\/s-0042-1749367"},{"key":"bibr8-10935266241281797","doi-asserted-by":"publisher","DOI":"10.1002\/mgg3.1465"},{"key":"bibr9-10935266241281797","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.63132"},{"key":"bibr10-10935266241281797","doi-asserted-by":"publisher","DOI":"10.1016\/j.ydbio.2007.02.007"},{"key":"bibr11-10935266241281797","doi-asserted-by":"publisher","DOI":"10.1038\/74307"},{"key":"bibr12-10935266241281797","doi-asserted-by":"publisher","DOI":"10.1086\/421053"},{"key":"bibr13-10935266241281797","doi-asserted-by":"publisher","DOI":"10.1086\/498879"},{"key":"bibr14-10935266241281797","doi-asserted-by":"publisher","DOI":"10.1093\/hmg\/ddn272"},{"key":"bibr15-10935266241281797","doi-asserted-by":"publisher","DOI":"10.1159\/000289817"},{"key":"bibr16-10935266241281797","doi-asserted-by":"publisher","DOI":"10.1093\/hmg\/ddt012"},{"key":"bibr17-10935266241281797","doi-asserted-by":"publisher","DOI":"10.1056\/NEJMoa1406829"},{"key":"bibr18-10935266241281797","doi-asserted-by":"publisher","DOI":"10.1038\/s41436-018-0377-x"},{"key":"bibr19-10935266241281797","doi-asserted-by":"publisher","DOI":"10.1007\/s12098-014-1493-5"}],"container-title":["Pediatric and Developmental Pathology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/journals.sagepub.com\/doi\/pdf\/10.1177\/10935266241281797","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/journals.sagepub.com\/doi\/full-xml\/10.1177\/10935266241281797","content-type":"application\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/journals.sagepub.com\/doi\/pdf\/10.1177\/10935266241281797","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,5,2]],"date-time":"2026-05-02T04:11:02Z","timestamp":1777695062000},"score":1,"resource":{"primary":{"URL":"https:\/\/journals.sagepub.com\/doi\/10.1177\/10935266241281797"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2024,9,26]]},"references-count":19,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2025,1]]}},"alternative-id":["10.1177\/10935266241281797"],"URL":"https:\/\/doi.org\/10.1177\/10935266241281797","relation":{},"ISSN":["1093-5266","1615-5742"],"issn-type":[{"value":"1093-5266","type":"print"},{"value":"1615-5742","type":"electronic"}],"subject":[],"published":{"date-parts":[[2024,9,26]]}}}