187 top medical experts on Weill-Marchesani Syndrome across 15 countries and 9 U.S. states, including 25 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Weill-Marchesani Syndrome: Rare congenital disorder of connective tissue characterized by brachydactyly, joint stiffness, childhood onset of ocular abnormalities (e.g., microspherophakia, ectopia lentis; glaucoma), and proportionate short stature. Cardiovascular anomalies are occasionally seen.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Connective Tissue Diseases (1,572), Dwarfism (1,222), Hereditary Eye Diseases (901), Multiple Abnormalities (3,208).
  4. Synonyms: Congenital Mesodermal Dysmorphodystrophy,  Spherophakia Brachymorphia Syndrome,  Weill Marchesani Syndrome,  Autosomal Recessive Weill-Marchesani Syndrome


  

        

                    


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