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Isolated hexadactylia: A rare case of central polydactyly of the foot

机译:孤立的六十腔:徒步徒步的罕见案例

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Background: Central polydactyly of foot is uncommon form of polydactyly but it usually causes intermetatarsal widening because of metatarsal bifurcation. Central polydactyly associated with T shaped bifurcation of meta-tarsal in vertical plane has not been reported yet.Case: We present a 4 year male child with extra toe on the dorsal aspect of right foot with complains of difficulty in wearing footwear and poor cosmesis. The extra digit was fully developed with bifurcation of 2nd metatarsal bone proximal to the head without any intermetatarsal widening. The angular deviation was 45° to the longitudinal axis of foot and in a plane vertical to the transverse arch of foot. The child was operated with excision of extra toe without any residual bony deformity.Conclusion: The central polydactyly is rare type of polydactyly of foot. Central polydactyly with metatarsal extension causing intermetatarsal widening has been well described entity. But the previous classifications need to be modified to include central polydactyly with vertical oriented T bifurcation of metatarsal bone without intermetatarsal widening.
机译:背景:足中央多指畸形是一种罕见的多指畸形,但由于跖骨分叉,它通常会导致跖骨间增宽。与垂直面上跖骨T形分叉相关的中央多指畸形尚未见报道。病例:我们报告一名4岁男童,右脚背侧多了一个脚趾,主诉穿鞋困难,美容效果差。额外的手指完全发育,第二跖骨分叉处靠近头部,没有任何跖骨间增宽。角度偏差与足纵轴呈45°角,且在垂直于足横弓的平面内。手术切除了多余的脚趾,没有任何残留的骨畸形。结论:中央多指是一种罕见的足部多指畸形。中央多指畸形伴跖骨延长,导致跖骨间增宽,这一点已得到充分描述。但是,以前的分类需要修改,以包括中央多指畸形和垂直方向的跖骨T分叉,而不伴有跖骨间增宽。

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