Herman T E, McAlister W H, Boniface A, Whyte M P
Mallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, Missouri.
Pediatr Radiol. 1992;22(5):363-5. doi: 10.1007/BF02016258.
Occipital horn syndrome, a rare genetic disorder of copper metabolism, was recognized in 2 unrelated patients. Radiographs of these patients at various ages allowed confirmation of previously described radiographic findings. In addition, new radiographic manifestations were encountered. These pathognomonic radiographic findings are presented and the clinical and biochemical features of occipital horn syndrome are reviewed.
枕角综合征是一种罕见的铜代谢遗传性疾病,在2例无亲缘关系的患者中得到确诊。对这些患者不同年龄段的X线片进行分析,证实了先前描述的影像学表现。此外,还发现了新的影像学表现。本文展示了这些具有诊断意义的影像学表现,并对枕角综合征的临床和生化特征进行了综述。