{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,9,19]],"date-time":"2025-09-19T06:59:11Z","timestamp":1758265151814,"version":"3.40.4"},"reference-count":7,"publisher":"BMJ","content-domain":{"domain":["bmj.com"],"crossmark-restriction":true},"short-container-title":["BMJ Case Reports"],"accepted":{"date-parts":[[2016,5,26]]},"abstract":"<jats:p>Tibial hemimelia (congenital longitudinal deficiency of the tibia) is rare (1 in 1\u2005000\u2005000). There are several classifications in the literature. We report an unclassified case of tibial hemimelia. A 6-year-old girl presented with shortening of the right lower limb, with a small rudimentary foot (presence of all toes) and hyper lax ankle. Quadriceps function was excellent. Radiograph showed a partial tibia and fibula in synostosis. The Jones and Kalamachi type 2 classifications both mention similar tibial anomalies; however, the fibula is normal in both varieties. The present variety can be considered as a variant of type 2 tibial hemimelia.<\/jats:p>","DOI":"10.1136\/bcr-2016-215305","type":"journal-article","created":{"date-parts":[[2016,6,8]],"date-time":"2016-06-08T15:37:09Z","timestamp":1465400229000},"page":"bcr2016215305","update-policy":"https:\/\/doi.org\/10.1136\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":3,"title":["Unclassified tibial hemimelia"],"prefix":"10.1136","volume":"2016","author":[{"given":"Vishnu","family":"Senthil","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Imthias V","family":"Kottamttavide","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hitesh","family":"Shah","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","published-online":{"date-parts":[[2016,6,8]]},"reference":[{"key":"2025042703313619000_2016.jun08_1.bcr2016215305.1","doi-asserted-by":"publisher","DOI":"10.1007\/s00264-003-0490-5"},{"key":"2025042703313619000_2016.jun08_1.bcr2016215305.2","doi-asserted-by":"crossref","first-page":"31","DOI":"10.1302\/0301-620X.60B1.627576","article-title":"Congenital aplasia and dysplasia of the tibia with intact fibula: classification and management","volume":"60","author":"Jones","year":"1978","journal-title":"J Bone Joint Surg Br"},{"key":"2025042703313619000_2016.jun08_1.bcr2016215305.3","doi-asserted-by":"crossref","first-page":"581","DOI":"10.1302\/0301-620X.67B4.4030854","article-title":"Congenital deficiency of the tibia","volume":"67","author":"Kalamachi","year":"1985","journal-title":"J Bone Joint Surg Br"},{"key":"2025042703313619000_2016.jun08_1.bcr2016215305.4","doi-asserted-by":"publisher","DOI":"10.1007\/s11832-008-0081-5"},{"key":"2025042703313619000_2016.jun08_1.bcr2016215305.5","first-page":"454","article-title":"Management of type 2 tibial hemimelia; short review on treatment of tibial defects and the results of four patient treated using a modified brown procedure","volume":"13","author":"Salal","year":"2014","journal-title":"Iraqi Postgrad Med J"},{"key":"2025042703313619000_2016.jun08_1.bcr2016215305.6","doi-asserted-by":"crossref","first-page":"893","DOI":"10.1302\/0301-620X.74B6.1447253","article-title":"Management and outcome in tibial dysplasia","volume":"74","author":"Pattinson","year":"1992","journal-title":"J Bone Joint Surg Br"},{"key":"2025042703313619000_2016.jun08_1.bcr2016215305.7","doi-asserted-by":"publisher","DOI":"10.1097\/BPO.0000000000000280"}],"container-title":["BMJ Case Reports"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/bcr-2016-215305","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,4,27]],"date-time":"2025-04-27T10:31:42Z","timestamp":1745749902000},"score":1,"resource":{"primary":{"URL":"https:\/\/casereports.bmj.com\/lookup\/doi\/10.1136\/bcr-2016-215305"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2016,6,8]]},"references-count":7,"alternative-id":["10.1136\/bcr-2016-215305"],"URL":"https:\/\/doi.org\/10.1136\/bcr-2016-215305","relation":{},"ISSN":["1757-790X"],"issn-type":[{"type":"electronic","value":"1757-790X"}],"subject":[],"published":{"date-parts":[[2016,6,8]]}}}