203 top medical experts on Campomelic Dysplasia across 18 countries and 12 U.S. states, including 19 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Campomelic Dysplasia: A congenital disorder of chondrogenesis and osteogenesis characterized by hypoplasia of endochondral bones. In most cases there is a curvature of the long bones especially the tibia with dimpling of the skin over the bowed areas, malformation of the pelvis and spine, 11 pairs of ribs, hypoplastic scapulae, club feet, micrognathia, cleft palate, tracheobronchomalacia, and in some patients male-to-female sex reversal (SEX reversal, gonadal). Most patients die in the neonatal period of respiratory distress. Campomelic dysplasia is associated with haploinsufficiency of the SOX9 transcription factor gene.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Musculoskeletal Abnormalities (2,763).


  

        

                    


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