Morgan C L, Gehweiler J A, Osborne R L
Rev Interam Radiol. 1977 Jan;2(1):49-52.
Two patients with the Weismann-Netter-Stuhl syndrome are presented, one with classic and widespread findings, the other with minimal changes. Subsequent to its initial description in the French literature seven cases have been reported in English. The syndrome is characterized by anterior bowing of the tibia and fibula with posterior cortical thickening and trabecular irregularity in the region of bowing. Other long bones may be similarly affected. Scoliosis and pelvic findings are frequent. Short stature is usually present. The syndrome appears to be a generalized diaphyseal dysplasia.
本文报告了两名患有魏斯曼 - 内特尔 - 施图尔综合征的患者，一名具有典型且广泛的表现，另一名仅有轻微变化。该综合征最初在法国文献中被描述，随后英文文献中报道了7例。该综合征的特征是胫腓骨前部弓形弯曲，弯曲部位后侧皮质增厚且小梁不规则。其他长骨可能也会受到类似影响。脊柱侧弯和骨盆改变很常见。通常存在身材矮小的情况。该综合征似乎是一种全身性骨干发育异常。
