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Torticollis due to a combination of sternomastoid contracture and congenital vertebral anomalies

机译:斜鼻肌挛缩症和先天性脊椎畸形的综合症

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摘要

We report four children with sternomastoid contracture combined with torticolis secondary to congenital vertebral anomalies. Two had features of Klippel-Feil syndrome and a proximal release of the contracted sternomastoid produced good cosmetic correction initially. Progression of the deformity occurred subsequently without recurrence of sternomastoid contracture. One child had such mild deformity that it was merely observed. The fourth child was born with torticollis without sternomastoid tightness and a vertebral anomaly was later recognised. He slowly developed a sternomastoid contracture and his condition was considerably improved by sternomastoid release. This combination of causes of torticollis has not, as far as we know, been previously reported. The clinician should be aware of it and should also realise that radiographs of the very immature spine may not disclose the bony anomalies.
机译:我们报告了四名儿童患有类固醇挛缩挛缩症合并继发于先天性椎体异常的斜颈。其中两个具有Klippel-Feil综合征的特征,收缩的胸骨乳突向近端释放最初产生了良好的美容矫正。随后发生畸形进展,而没有乳突肌挛缩的复发。一个孩子有如此轻度的畸形,仅能被观察到。第四个孩子出生时患有斜颈,没有胸锁乳突肌紧缩,后来发现椎骨异常。他缓慢发展为胸锁乳突肌挛缩症,并通过胸锁乳突肌释放明显改善了病情。据我们所知,以前没有报道过这种斜颈原因的组合。临床医生应该意识到这一点,并且还应该意识到,非常不成熟的脊柱的X光片可能无法揭示骨异常。
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