{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,25]],"date-time":"2026-08-25T08:52:44Z","timestamp":1787647964227,"version":"build-2736575974"},"reference-count":6,"publisher":"BMJ","content-domain":{"domain":["bmj.com"],"crossmark-restriction":true},"short-container-title":["BMJ Case Reports"],"accepted":{"date-parts":[[2016,8,2]]},"abstract":"<jats:p>Tibial hemimelia is a rare congenital limb deficiency which is characterised by a hypoplastic\/aplastic tibia. It actually represents a spectrum of anomalies, ranging from mild hypoplasia of the tibia to total absence of the tibia. Several classifications based on radiological description exist in the literature. The tibial hemimelia is usually described with preaxial mirror polydactyly, split hand\/foot syndrome\u2014ectrodactyly, polydactyly\u2014triphalangeal thumb syndrome (Werner syndrome) and micromelia\u2013trigonal brachycephaly syndrome. We describe a child with unclassified tibial hemimelia. The child had right incomplete tibial hemimelia with bifid tibia, left complete tibial hemimelia, bilateral split hands and left split foot. This is the first report of the bifid tibia in the literature.<\/jats:p>","DOI":"10.1136\/bcr-2016-216622","type":"journal-article","created":{"date-parts":[[2016,8,16]],"date-time":"2016-08-16T15:56:30Z","timestamp":1471362990000},"page":"bcr2016216622","update-policy":"https:\/\/doi.org\/10.1136\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":5,"title":["Tibial hypoplasia with a bifid tibia: an unclassified tibial hemimelia"],"prefix":"10.1136","volume":"2016","author":[{"given":"Krupa","family":"Shah","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hitesh","family":"Shah","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"239","published-online":{"date-parts":[[2016,8,16]]},"reference":[{"key":"2025042703530284000_2016.aug16_1.bcr2016216622.1","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":"2025042703530284000_2016.aug16_1.bcr2016216622.2","doi-asserted-by":"crossref","first-page":"581","DOI":"10.1302\/0301-620X.67B4.4030854","article-title":"Congenital deficiency of the tibia","volume":"67","author":"Kalamchi","year":"1985","journal-title":"J Bone Joint Surg Br"},{"key":"2025042703530284000_2016.aug16_1.bcr2016216622.3","doi-asserted-by":"publisher","DOI":"10.1007\/s11832-008-0081-5"},{"key":"2025042703530284000_2016.aug16_1.bcr2016216622.4","doi-asserted-by":"publisher","DOI":"10.1007\/s11832-006-0001-5"},{"key":"2025042703530284000_2016.aug16_1.bcr2016216622.5","doi-asserted-by":"publisher","DOI":"10.1136\/jmedgenet-2011-100409"},{"key":"2025042703530284000_2016.aug16_1.bcr2016216622.6","doi-asserted-by":"publisher","DOI":"10.1097\/BPB.0b013e3283620640"}],"container-title":["BMJ Case Reports"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/bcr-2016-216622","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,4,27]],"date-time":"2025-04-27T10:53:11Z","timestamp":1745751191000},"score":1,"resource":{"primary":{"URL":"https:\/\/casereports.bmj.com\/lookup\/doi\/10.1136\/bcr-2016-216622"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2016,8,16]]},"references-count":6,"alternative-id":["10.1136\/bcr-2016-216622"],"URL":"https:\/\/doi.org\/10.1136\/bcr-2016-216622","relation":{},"ISSN":["1757-790X"],"issn-type":[{"value":"1757-790X","type":"electronic"}],"subject":[],"published":{"date-parts":[[2016,8,16]]}}}