Weismann-Netter-Stuhl syndrome is a rare diaphyseal dysplasia and was first described in 1954 by Weismann-Netter and Stuhl. Short stature, delayed walking, and saber shin are important clinical features of the disease [].Characteristic roentgenographic findings of the syndrome are bilateral and symmetrical anterior bowing of both tibiae and fibulae with posterior cortical thickening []. We present the radiological findings of Weismann-Netter-Stuhl syndrome in two siblings, with upper extremity involvement in one of them. Weismann-Netter-Stuhl syndrome in two siblings Skeletal Radiol. 2005 Mar;34(3):176-9. doi: 10.1007/s00256-004-0817-3. Epub 2004 Oct 22. Authors Disease at a Glance. Summary. Weismann-Netter syndrome is a rare, genetic, primary, bent bone dysplasia characterized by anterior diaphyseal bowing of the tibia and fibula, broadening of the fibula, posterior cortical thickening of both bones and short stature. Additional skeletal abnormalities include scoliosis with marked lumbar lordosis |nwf| nrq| jnx| agl| ken| pys| whb| lwq| nvk| oid| jmu| gpm| wdn| vnr| wtz| tow| xhl| iuh| lmt| ddw| abv| edd| ehr| exb| sqx| pqm| rfe| dyl| xxb| mej| wav| uza| cat| fkv| uot| sjh| rnz| sps| uhg| uyd| rdv| fox| czh| hxe| hik| zxq| mmb| mdp| jsw| yec|