131 top medical experts on Ter Haar syndrome across 10 countries and 1 U.S. states, including 9 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Ter Haar syndrome: A rare primary bone dysplasia characterized by megalocornea, multiple skeletal anomalies, characteristic facial dysmorphism (wide fontanels, prominent forehead, hypertelorism, prominent eyes, full cheeks and micrognathia) and developmental delay.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Frank Ter Haar syndrome,  Frank-Ter Haar Syndrome,  and developmental delay multiple skeletal anomalies Megalocornea


  

        

                    


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