罕见足印:孤立前轴完全发育多余脚趾1例报告。

Varun Kumar, Mohan Choudhary, Srinivasan Rajappa, Kevin Lourdes, Arjun Ganesh, P Velmurugan
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引用次数: 0

摘要

足多指畸形,尤其是前轴多指畸形,是一种罕见的先天性畸形,可伴随各种先天性异常和综合征发生。多指畸形的分类,如Venn-Watson系统,有助于理解这种先天性疾病的复杂性和可变性。病例报告:本病例报告详细介绍了一名5岁男孩的前轴多指畸形的表现和手术干预,其特征是右脚副趾,自出生以来就阻碍了他正常行走的能力,并通过手术切除以获得更好的生活。结论:足前轴多指畸形是一种罕见的先天性畸形,严重影响足的活动能力和生活质量。早期诊断,辅以详细的临床评估和放射成像,对适当的治疗至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Rare Footprint: A Case Report of Isolated Pre-Axial Fully Developed Supernumerary Toe.

Introduction: Polydactyly of the foot, particularly pre-axial polydactyly, is a rare congenital malformation that can occur alongside various congenital anomalies and syndromes. Classification of polydactyly, such as Venn-Watson's system, aids in understanding the complexity and variability of this congenital condition.

Case report: This case report details the presentation and surgical intervention of a 5-year-old boy with pre-axial polydactyly characterized by an accessory toe on the right foot, which had hindered his ability to walk properly since birth and his journey through surgical excision for a better stand in life.

Conclusion: Pre-axial polydactyly of the foot is a rare congenital anomaly that can significantly affect mobility and quality of life. Early diagnosis, aided by a detailed clinical evaluation and radiographic imaging, is crucial for appropriate management.

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