Babeau P, Tiré J, Pras P, Serres J
J Radiol Electrol Med Nucl. 1977 Oct;58(10):605-8.
The authors report two cases of individuals sufferring from bow-leggedness, which they attribute to tibio-fibular thoxo-pachyosteosis. On the basis of these new cases, they review the radioclinical characteristics of the diagnosis of Weismann-Netter and Stuhl tibio-fibular toxo-pachy-osteosis. This dysmorphic syndrome is usually familial, very likely of genetic origin, and characterised by the small stature of those affected with curving of the tibia and fibula with an anterior convexity and thickening of the posterior cortex of the bony diaphysis. This clinical and radiological individuality permits its differential diagnosis from rickets and congenital syphilis, with which it was long confused. This dysmorphy causes no problems and therefore requires no general treatment.
作者报告了两例患有弓形腿的病例，他们将其归因于胫腓骨结核性厚骨炎。基于这些新病例，他们回顾了魏斯曼 - 内特尔和施图尔胫腓骨结核性厚骨炎诊断的放射临床特征。这种畸形综合征通常具有家族性，很可能起源于遗传，其特征是受影响者身材矮小，胫骨和腓骨弯曲，骨干后皮质增厚并向前凸出。这种临床和放射学特征使其能够与佝偻病和先天性梅毒进行鉴别诊断，它曾长期与这两种疾病混淆。这种畸形不会引起问题，因此不需要进行一般治疗。
