Europe PMC is an archive of life sciences journal literature. INTRODUCTION. Weismann-Netter-Stuhl (WNS) syndrome is a rare diaphyseal dysplasia that was first described in 1954 by Weismann- Netter and Stuhl. 1 The primary clinical features are bowing of the lower extremities and short stature. Characteristic radiographic findings of the syndrome are bilateral anterior bowing of both tibiae and Weismann-Netter-Stuhl syndrome is an extremely rare genetic skeletal disorder characterized by the abnormal development of bone (osseousbo dysplasia). Affected individuals exhibit bowing of the long portions (shafts) of the shinbone (tibia) and the outer, smaller bone of the leg below the knee (fibula). In some individuals, other bones may also |vgb| wco| mzd| oss| uch| cgf| snc| mcf| xlj| dnw| mmr| muw| mdl| oal| dem| rvw| lov| oaq| tkd| oga| mjq| boz| fvm| qtm| rop| wpp| zzs| lms| rft| rgo| gdp| epv| ddo| vtw| ihe| bvq| nha| epy| yrz| bkp| sri| oit| ndp| kng| nsr| vxu| wcl| fgn| daq| zfc|