8 top medical experts on Weismann Netter syndrome across 1 countries, including 1 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Weismann Netter syndrome: 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, horizontal sacrum and square iliac wings and/or, less frequently, vertebral malformations, abnormal shape of the clavicles and ribs, calvarial hyperostosis and delayed eruption of permanent teeth. Delayed ambulation is also frequently associated.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Anterior bowing of legs with dwarfism,  with dwarfism anterior Bowing of legs,  Toxopachyosteose diaphysaire tibio-peroniere,  Toxopachyosteosis,  Toxopachyoteose diaphysaire tibio peroniere,  Weismann Netter Stuhl syndrome,  Weismann-Netter Syndrome


  

        

                    


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