Long-term follow-up of congenital distal tibiofibular diastasis: a report of two female patients. (CROSBI ID 277344)
Prilog u časopisu | ostalo | međunarodna recenzija
Podaci o odgovornosti
Skolan V, Šmigovec I, Ðapić T, Antičević D
engleski
Long-term follow-up of congenital distal tibiofibular diastasis: a report of two female patients.
Congenital diastasis of the inferior tibiofibular joint is an extremely rare variant of dysplastic tibial anomaly, which is usually associated with significant shortening of the lower leg and ipsilateral foot deformity due to talus incarceration in the distal tibiofibular mortise. The purpose of this study was to present the long-term results of reconstructive treatment and the functional outcome after a follow-up of 11-16 years. The principles of extremity preservation and reconstruction with the Ilizarov frame have shown a stable ankle joint, a plantigrade foot, and fully independent outdoor ambulation in both patients at the final follow-up. We concluded that amputation should not be performed under this condition.
congenital ; distal tibio-fibular diastasis ; long-term, surgery
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Podaci o izdanju
22 (5)
2013.
464-469
objavljeno
1060-152X
1473-5865
10.1097/BPB.0b013e32835e046f