下肢罕见的前轴多指畸形。1例报告及文献回顾

Mariano Tovar Ponce, Mauricio Martinez Hurtado, Jose David Simonin Lopez, David Gonzalez Garcia, Claudia Monserrat Perez Quintanar, Jazmin Danae Chavez Hernandez, Horacio Sanchez Espinosa, Carlos Roberto Perez Garcia, Emmanuel Stephano Bracho Ruiz
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引用次数: 0

摘要

这种被称为小儿足多指畸形的情况可以表现为多种畸形,从一个多出的手指只通过一根薄薄的结缔组织带与足的其余部分相连,到复杂的足中央重复,包括跗骨的重复。脚的前轴多指畸形的表现是至关重要的理解,即使它是相当罕见的。这是因为在超过一半的情况下,一些先天性畸形,如并指和房间隔缺陷,已被描述。手术重建的结果应该是一个稳定,活动,无痛的脚,有五个美观的脚趾。这应该允许患者穿标准的鞋子和走路没有任何不适。
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Lower Extremity Rare Preaxial Polydactyly. A Case Report and Literature Review
The condition known as pediatric foot polydactyly can manifest itself in a broad range of malformations, from a single extra digit that is only connected to the rest of the foot by a thin band of connective tissue to intricate central foot duplications that involve the duplication of tarsal bones. The presentation of preaxial polydactyly of the foot is crucial to understand, even though it is quite uncommon. This is because in over half of the cases, several congenital malformations, such as syndactyly and atrial septum defects, have been described. The result of surgical reconstruction should be a foot that is stable, mobile, and pain-free, with five aesthetically pleasing toes. This should allow the patient to wear standard footwear and walk without experiencing any discomfort.
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