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tibial hemimelia

Friday 29 December 2006

Tibial hemimelia is a rare congenital anomaly characterized by deficiency of the tibia with relatively intact fibula. Tibial hemimelia is identified as a solitary disorder, or a part of more complex malformation syndromes. Although the majority of cases with tibial hemimelia are sporadic, affected families with possible autosomal dominant or autosomal recessive inheritance have been reported.

TYpes

- sporadic forms
- syndromal forms

  • Gollop-Wolfgang complex
  • tibial agenesis-ectrodactyly syndrome

See also

- tibial malformations