{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,26]],"date-time":"2026-08-26T14:43:22Z","timestamp":1787755402024,"version":"build-2784847793"},"reference-count":9,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"4","content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"abstract":"<jats:sec>\n                    <jats:title>Case:<\/jats:title>\n                    <jats:p>An infant boy with chondrodysplasia punctata tibial-metacarpal type (CDP-TM) was followed up till skeletal maturity. The patient underwent surgeries for bilateral patellar dislocations at the age of 9 years of age, left leg length discrepancy at 12 years, and atlantoaxial subluxation at 14 years. At the final follow-up at 18 years, he had no complaints or limitation of his daily life activities.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion:<\/jats:title>\n                    <jats:p>CDP-TM may require multiple orthopedic surgeries such as patellofemoral instability, limb length discrepancy, and upper cervical dysplasia until skeletal maturity, and should be followed in order to identify them early.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.2106\/jbjs.cc.22.00332","type":"journal-article","created":{"date-parts":[[2023,2,23]],"date-time":"2023-02-23T10:06:27Z","timestamp":1677146787000},"update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":1,"title":["Surgical Treatment of Chondrodysplasia Punctata Tibial-Metacarpal Type Until Skeletal Maturity"],"prefix":"10.2106","volume":"12","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-5036-0408","authenticated-orcid":false,"given":"Yoh","family":"Fujimoto","sequence":"first","affiliation":[{"name":"Department of Pediatric Orthopedics, Shizuoka Children's Hospital, Shizuoka, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-2051-3538","authenticated-orcid":false,"given":"Kazuharu","family":"Takikawa","sequence":"additional","affiliation":[{"name":"Department of Pediatric Orthopedics, Shizuoka Children's Hospital, Shizuoka, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-1088-2006","authenticated-orcid":false,"given":"Yujiro","family":"Takeshita","sequence":"additional","affiliation":[{"name":"Department of Orthopaedic Surgery, Yokohama Rosai Hospital, Kanagawa, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","published-online":{"date-parts":[[2022,10]]},"reference":[{"issue":"12","key":"bib1-20240805","doi-asserted-by":"crossref","first-page":"2393","DOI":"10.1002\/ajmg.a.61366","article-title":"Nosology and classification of genetic skeletal disorders: 2019 revision","volume":"179","author":"Mortier","year":"2019","journal-title":"Am J Med Genet A."},{"issue":"2","key":"bib2-20240805","doi-asserted-by":"crossref","first-page":"148","DOI":"10.1002\/ajmg.a.20383","article-title":"Longterm follow-up in chondrodysplasia punctata, tibia-metacarpal type, demonstrating natural history","volume":"124a","author":"Savarirayan","year":"2004","journal-title":"Am J Med Genet A."},{"issue":"2","key":"bib3-20240805","doi-asserted-by":"crossref","first-page":"200","DOI":"10.1002\/ajmg.1320370208","article-title":"Chondrodysplasia punctata, tibia-metacarpal (MT) 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punctata","volume":"20","author":"Morota","year":"2017","journal-title":"J Neurosurg Pediatr."},{"issue":"9","key":"bib7-20240805","doi-asserted-by":"crossref","first-page":"e680","DOI":"10.1097\/BPO.0000000000001014","article-title":"Cervical spine deformities in children with rhizomelic chondrodysplasia punctata","volume":"39","author":"Abousamra","year":"2019","journal-title":"J Pediatr Orthop."},{"issue":"7","key":"bib8-20240805","doi-asserted-by":"crossref","first-page":"1346","DOI":"10.1007\/s00586-011-2083-0","article-title":"Complications and outcomes of posterior fusion in children with atlantoaxial instability","volume":"21","author":"Tauchi","year":"2012","journal-title":"Eur Spine J."},{"key":"bib9-20240805","first-page":"5974281","article-title":"Successful treatment of atlantoaxial subluxation in an adolescent patient with brachytelephalangic chondrodysplasia punctata","volume":"2019","author":"Fujimoto","year":"2019","journal-title":"Case Rep Orthop."}],"container-title":["JBJS Case Connector"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.ovid.com\/10.2106\/JBJS.CC.22.00332","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,8,26]],"date-time":"2026-08-26T13:42:31Z","timestamp":1787751751000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.ovid.com\/10.2106\/JBJS.CC.22.00332"}},"subtitle":["A Case Report"],"short-title":[],"issued":{"date-parts":[[2022,10]]},"references-count":9,"journal-issue":{"issue":"4","published-online":{"date-parts":[[2022]]}},"URL":"https:\/\/doi.org\/10.2106\/jbjs.cc.22.00332","relation":{},"ISSN":["2160-3251"],"issn-type":[{"value":"2160-3251","type":"electronic"}],"subject":[],"published":{"date-parts":[[2022,10]]},"assertion":[{"value":"2022-05-04","name":"received","label":"Received","group":{"name":"publication_history","label":"Publication 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