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Congenital Kyphosis in Thoracic Spine Secondary to Absence of Two Thoracic Vertebral Bodies

机译:缺乏两个胸椎体继发于胸椎的先天性后凸畸形

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摘要

Congenital thoracic kyphosis at D6-D7 vertebral body level has been encountered in an 18-month-old boy without neurological deficit. The constellation of the spine malformation complex such as incomplete development of the vertebral bodies associated with defective ossification of the thoracic pedicles causing effectively the development of spinal cord injury at the kyphotic level of D6-D7 were present. Congenital kyphosis in thoracic spine secondary to absence of two thoracic vertebral bodies has been reported in a few studies. It is the absence and asymmetry of growth plates that may contribute to a congenital defect. Congenital Kyphosis refers to the normal convex curvature of the spine as it occurs in the thoracic and sacral regions since birth. Congenital kyphosis is an uncommon, but potentially devastating anomaly of the spine. It is one of the important aetiology for spinal cord compression leading to further neurological complications. Congenital kyphosis although rare, is more associated with neurological complication. Early identification not only helps in understanding its natural history but also helps in deciding its management.
机译:在一个没有神经系统缺陷的18个月大男孩中,遇到了D6-D7椎体水平的先天性胸椎后凸畸形。存在脊椎畸形复合体的星座,例如与椎弓根骨化不良相关的椎体发育不全,导致在D6-D7的后凸水平有效导致脊髓损伤的发展。在一些研究中,已经报告了由于缺少两个胸椎体而导致的胸椎先天性后凸畸形。生长板的缺乏和不对称可能导致先天性缺陷。先天性后凸畸形是指自出生以来在胸部和骨区域出现的正常脊柱凸曲率。先天性后凸畸形不常见,但可能会破坏脊柱。它是导致进一步神经系统并发症的脊髓压迫的重要病因之一。先天性后凸畸形虽然很少见,但与神经系统并发症有关。早期识别不仅有助于了解其自然历史,而且有助于决定其管理。

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