Gutiérrez Macías A, Rodríguez Peñalver M, Carrión Ojanguren M A, Rodríguez López F
An Esp Pediatr. 1979 Nov;12(11):801-6.
A two-years-old male with toxopachyosteose diaphisaire tibioperoniere (Weismann-Netter syndrome) is presented. First observation of this syndrome in spanish publications. Basic signs of this syndrome: dwarfism with bilateral tibio-fibula incurvation and sclerosis, are remembered, as well as deafness like associated symptom. Radiologic signs to differentiate between others process, specially rickets and syphilis, with which it was for a long time confused, are remarked.
本文介绍了一名患有胫腓骨干骺端骨肥厚（魏斯曼 - 内特尔综合征）的两岁男性患儿。这是西班牙出版物中对该综合征的首次观察报道。文中回顾了该综合征的基本体征：双侧胫腓骨弯曲和硬化导致的侏儒症，以及作为相关症状的耳聋。还提到了用于区分其他病症，特别是长期与之混淆的佝偻病和梅毒的放射学体征。
