首页> 外文期刊>Journal of Orthopaedic Translation >Letter to the editor concerning “Imbalanced development of anterior and posterior thorax is a causative factor triggering scoliosis” by Chen et?al., Journal of Orthopaedic Translation, 2019, https://doi.org/10.1016/j.jot.2018.12.001
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Letter to the editor concerning “Imbalanced development of anterior and posterior thorax is a causative factor triggering scoliosis” by Chen et?al., Journal of Orthopaedic Translation, 2019, https://doi.org/10.1016/j.jot.2018.12.001

机译:关于编辑的关于“前后和后胸部的不平衡发展是一种致病因子触发脊柱侧凸”的信,骨科翻译杂志,2019,https:// doi .org / 10.1016 / J.JOT.2018.12.001

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With great interest, we have read “Imbalanced development ofanterior and posterior thorax is a causative factor triggering scoliosis” byChen et al. [1] and would like to compliment the authors on their article.In this article, the authors described a theory about the origin of idio-pathicscoliosis,a topic thathas receivedmuch interestovera long periodof time. Patients with scoliosis were found to have a reduced thoracicanteroposterior length ratio, resulting from the relatively longer thoracicvertebra and relatively shorter sternum. In addition, artificially reducingthe thoracic anteroposterior length ratio by surgically destroying thesternal growth plates induces scoliosis in quadrupedal mice and even amore increased scoliosis curvature in bipedal mice. Consistently, micewith deficiency of fibroblast growth factor receptor 3, which had severescoliosis, had a reduced thoracic anteroposterior length ratio. The au-thors interpreted these findings as an imbalanced growth between thethoracic vertebral column and the sternum that may also play a role inthe pathogenesis of idiopathic scoliosis. Their hypothesis was that thegradually reduced relative length of the sternum induced scoliosis.
机译:非常兴趣,我们已阅读“患有李内和后胸部的不平衡的发展是一种致病因素触发脊柱侧凸”Bychen等。 [1]并希望赞美作者在他们的文章中。在本文中,作者描述了一个关于IDIO-PATOSCOLIOS的起源的理论,这是一个主题,即收到的时间很长一段时间。发现脊柱侧凸的患者具有降低的胸腺癌细胞增长率,由ThoracicVertebra相对较长的胸腺和胸骨相对较短。此外,人工通过手术摧毁史基生长板的胸腔前剂量长度比例,诱导Quadrupedal小鼠中的脊柱侧凸,甚至是双对小鼠中的脊柱侧凸曲率增加。始终如一地,缺乏缺血性血管症的成纤维细胞生长因子受体3的小鼠具有降低的胸腔前后长度比。 Au-Thirs将这些发现称为雌性椎体柱和胸骨之间的不平衡生长,也可能发挥特发性脊柱侧凸的发病机制。他们的假设是胸骨诱导脊柱侧凸的相对长度的二次上降。

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