Sivaji Akshaya Rathin, Kizhakkemuriyil Scaria Tony, Sundaramurthi Indumathi
Internal Medicine, Panimalar Medical College Hospital & Research Institute, Chennai, IND.
Anatomy, Panimalar Medical College Hospital & Research Institute, Chennai, IND.
Cureus. 2024 Sep 5;16(9):e68731. doi: 10.7759/cureus.68731. eCollection 2024 Sep.
Morton's foot syndrome is a hereditary condition characterized by a short first metatarsal compared to the second metatarsal. It often remains asymptomatic but can present with secondary complications. We report a case of a 46-year-old female presenting with Morton's foot syndrome, initially admitted for fatigue and weakness. Physical examination revealed characteristic foot deformities and multiple plantar calluses. This case highlights the anatomical features, pathophysiology, and biomechanical implications of Morton's foot syndrome. We discuss the challenges in differentiating between normal foot structure and Morton's foot, along with potential complications and strategies for effective management. This case report enhances understanding of Morton's foot syndrome, emphasizing the importance of recognizing this condition in clinical practice to prevent potential complications and provide appropriate management.
莫顿足综合征是一种遗传性疾病，其特征是第一跖骨比第二跖骨短。它通常没有症状，但可能会出现继发性并发症。我们报告一例46岁女性患有莫顿足综合征，最初因疲劳和虚弱入院。体格检查发现了典型的足部畸形和多个足底胼胝。本病例突出了莫顿足综合征的解剖学特征、病理生理学及生物力学影响。我们讨论了区分正常足部结构与莫顿足的挑战，以及潜在并发症和有效管理策略。本病例报告增进了对莫顿足综合征的理解，强调了在临床实践中识别该疾病以预防潜在并发症并提供适当管理的重要性。
