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| Content Provider | World Health Organization (WHO)-Global Index Medicus |
|---|---|
| Author | Kottamttavide, Imthias V. Senthil, Vishnu Shah, Hitesh |
| Description | Author Affiliation: Senthil V ( Department of Orthopedics, Kasturba Medical College, Manipal University, Manipal, Karnataka, India.); Kottamttavide IV ( Department of Orthopedics, Kasturba Medical College, Manipal University, Manipal, Karnataka, India.); Shah H ( Department of Orthopedics, Kasturba Medical College, Manipal University, Manipal, Karnataka, India.) |
| Abstract | Tibial hemimelia (congenital longitudinal deficiency of the tibia) is rare (1 in 1â 000â 000). 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. |
| Journal | BMJ Case Reports |
| Volume Number | 2016 |
| e-ISSN | 1757790X |
| Language | English |
| Publisher | BMJ Publishing Group Ltd. |
| Publisher Place | Great Britain (UK) |
| Access Restriction | One Nation One Subscription (ONOS) |
| Subject Keyword | Multidisciplinary |
| Content Type | Text |
| Resource Type | Article |
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