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Pycnodysostosis with Multi-Segmental Spinal Canal Stenosis due to Ossification of the Yellow Ligament

机译:黄韧带骨化引起的多节段性椎管狭窄症

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摘要

Pycnodysostosis is an autosomal recessive disorder characterized by osteosclerosis, small stature, acro-osteolysis of the distal phalanges, loss of the mandibular angle, separated cranial sutures with open fontanels, and frequent fractures. One identified cause of the disease is reduced activity of the cysteine protease cathepsin K. A 48-year-old woman with a history of frequent fractures presented with a severe gait disturbance. Radiography, computed tomography, magnetic resonance imaging, and gene analysis were performed. Physical examination revealed open fontanels, and radiographs showed increased bone density. DNA sequence analysis revealed a deletion mutation of the cathepsin K gene. We diagnosed pycnodysostosis based on these findings. The magnetic resonance and computed tomography images demonstrated multilevel spinal canal stenosis due to ossification of the yellow ligament. We performed a laminectomy, and the patient's neurological signs and symptoms improved. To our knowledge, this is the first case of pycnodysostosis with ossification of the yellow ligament.
机译:碧萝ody(Pycnodysostosis)是一种常染色体隐性遗传疾病,其特征为骨硬化,身材矮小,远端指骨的肢端骨溶解,下颌角丢失,颅骨缝线分开,font门开放以及频繁骨折。该疾病的一个确定原因是半胱氨酸蛋白酶组织蛋白酶K的活性降低。一名48岁的女性,有频繁骨折的历史,步态受到严重干扰。进行了放射线照相,计算机断层扫描,磁共振成像和基因分析。体格检查发现font门开放,X光片显示骨密度增加。 DNA序列分析显示组织蛋白酶K基因的缺失突变。基于这些发现,我们诊断出脓毒症。磁共振和计算机断层扫描图像显示由于黄韧带骨化导致多级椎管狭窄。我们进行了椎板切除术,患者的神经系统症状和体征得到改善。据我们所知,这是第一例黄韧带骨化的脓性囊肿病。

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