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CASE REPORT
Tibial hypoplasia with a bifid tibia: an unclassified tibial hemimelia
  1. Krupa Shah1,
  2. Hitesh Shah2
  1. 1Department of Obstetrics and Gynaecology, Kasturba Medical College, Manipal University, Manipal, Udupi, Karnataka, India
  2. 2Department of Orthopaedics, Kasturba Medical College, Manipal University, Manipal, Karnataka, India
  1. Correspondence to Dr Hitesh Shah, hiteshshah12{at}gmail.com

Summary

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—ectrodactyly, polydactyly—triphalangeal thumb syndrome (Werner syndrome) and micromelia–trigonal 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.

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