Verloes A, Muller C, Philippet P
Wallonia Centre for Human Genetics, Liège University, Liège, Belgium.
Am J Med Genet. 2000 Dec 18;95(5):473-6.
We report on an apparently normal child who shows hypopaplasia of the vertebral pedicles and posterior arches of several cervical, thoracic, and lumbar vertebrae with normally fused spinous apophyses, hypoplastic sacrum, lumbar epidural lipomatosis, synostoses of some cervical vertebral disks, and sacral spina bifida. The most likely mechanism is an abnormal differentiation of the spinal processes, due most probably to an absence of differentiation in cartilage of the dense mesenchyme forming their most anterior part. Because the anomalies affect multiple levels, we highly suspect a genetic basis to this unusual dysostosis affecting the development of the posterior sclerotomes.
我们报告了一名外表正常的儿童,其多个颈椎、胸椎和腰椎的椎弓根及后弓发育不全,棘突联合正常,骶骨发育不全,腰椎硬膜外脂肪增多症,部分颈椎间盘融合,以及骶骨脊柱裂。最可能的机制是脊柱结构异常分化,极有可能是由于形成其最前部的致密间充质软骨缺乏分化所致。由于这些异常影响多个层面,我们高度怀疑这种影响后体节发育的罕见骨发育异常存在遗传基础。