Brown L M, Robson M J, Sharrard W J
J Bone Joint Surg Br. 1980 Aug;62(3):291-6. doi: 10.1302/0301-620X.62B3.7410459.
Eleven patients with arthrogryposis multiplex congenita neurologica have been reviewed. Distinct patterns of deformity and muscle activity were identified which have been correlated with specific levels of segmental neurological motor deficit without sensory loss. The clinical picture was consistent with localised lesions of the anterior horn cell cell columns. This finding agreed with the recorded pathological lesions. Orthopaedic treatment should take account of the paralytic nature of the deformities.
对11例先天性多发性关节挛缩神经病患者进行了回顾性研究。确定了不同的畸形模式和肌肉活动情况，这些与节段性神经运动功能缺损的特定水平相关，且无感觉丧失。临床表现与前角细胞柱的局限性病变一致。这一发现与记录的病理病变相符。骨科治疗应考虑到畸形的麻痹性质。
