{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,26]],"date-time":"2026-08-26T14:41:44Z","timestamp":1787755304552,"version":"build-2784847793"},"reference-count":14,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"3","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["JBJS Case Connector"],"published-print":{"date-parts":[[2017,9]]},"abstract":"<jats:sec>\n                    <jats:title>Case:<\/jats:title>\n                    <jats:p>Trevor disease (dysplasia epiphysealis hemimelica [DEH]) is a rare, intra-articular anomaly of cartilaginous overgrowth of the epiphysis. The usual presentation is on 1 side of the body and on 1 side of the epiphysis. The natural history of this disease is not clear because the lesions often are treated during childhood. Additionally, hip involvement is relatively uncommon; to our knowledge, total hip arthroplasty in a patient with DEH has not been reported previously. Our patient presented with previously untreated DEH of the hip joint, which had developed into a very unusual shape. He was treated with a total hip arthroplasty and had satisfactory functioning 2.5 years postsurgery.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion:<\/jats:title>\n                    <jats:p>Untreated DEH of the hip can lead to a very misshapen hip with a deformed femoral head and loss of the shape of the acetabulum, as well as stiffness due to an unusual shape and osteoarthritic changes. A total hip arthroplasty can give satisfactory functional results.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.2106\/jbjs.cc.16.00277","type":"journal-article","created":{"date-parts":[[2017,9,13]],"date-time":"2017-09-13T19:18:54Z","timestamp":1505330334000},"page":"e67-e67","source":"Crossref","is-referenced-by-count":7,"title":["The Natural History of the Development of Trevor Disease of the Hip and Subsequent Arthroplasty"],"prefix":"10.2106","volume":"7","author":[{"given":"Gholam Hossain","family":"Shahcheraghi","sequence":"first","affiliation":[{"name":"Department of Orthopaedic Surgery, Bone and Joint Diseases Research Center, Shiraz University of Medical Sciences, Shiraz, Iran"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-5825-8993","authenticated-orcid":false,"given":"Mahzad","family":"Javid","sequence":"additional","affiliation":[{"name":"Department of Orthopaedic Surgery, Bone and Joint Diseases Research Center, Shiraz University of Medical Sciences, Shiraz, Iran"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","published-online":{"date-parts":[[2017,9,13]]},"reference":[{"issue":"1","key":"bib1-20230712","doi-asserted-by":"crossref","first-page":"237","DOI":"10.1302\/0301-620X.38B1.237","article-title":"Dysplasia epiphysialis hemimelica (tarso-ephiphysial aclasis)","volume":"38-B","author":"Fairbank","year":"1956","journal-title":"J Bone Joint Surg Br."},{"issue":"4","key":"bib2-20230712","doi-asserted-by":"crossref","first-page":"746","DOI":"10.2106\/00004623-196648040-00007","article-title":"Dysplasia epiphysealis hemimelica. 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