Bill P L, Versfeld G A
J Pediatr Orthop. 1982 Jun;2(2):139-42. doi: 10.1097/01241398-198202020-00004.
Twenty-five patients with congenital idiopathic clubfoot, aged 1 day to 22 months, were studied electromyographically. No myopathic or neurogenic changes were found in tibialis anterior, peroneus, gastrocnemius, extensor digitorum brevis, and abductor hallucis brevis muscles of the leg and foot. Maximum motor nerve conduction velocities for the peroneal and tibial nerves were normal. It is concluded that conventional electromyographic techniques were unable to demonstrate abnormalities suggesting neuropathic or myopathic changes in idiopathic clubfoot.
对25例年龄从1天至22个月的先天性特发性马蹄内翻足患儿进行了肌电图研究。在小腿和足部的胫前肌、腓骨肌、腓肠肌、趾短伸肌和拇短展肌中未发现肌病性或神经源性改变。腓总神经和胫神经的最大运动神经传导速度正常。结论是，传统肌电图技术无法显示提示特发性马蹄内翻足存在神经病变或肌病性改变的异常情况。
