53 top medical experts on Grebe type Chondrodysplasia across 8 countries and 1 U.S. states, including 5 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Grebe type Chondrodysplasia: A rare autosomal recessive acromesomelic dysplasia characterized by severe dwarfism at birth, abnormalities confined to limbs, severe shortening and deformity of long bones, fusion or absence of carpal and tarsal bones, ball shaped fingers and, occasionally, polydactyly and absent joints. As seen in acromesomelic dysplasia, Hunter-Thomson type and acromesomelic dysplasia, Maroteaux Type, facial features and intelligence are normal.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Brazilian Achondrogenesis,  Grebe type Acromesomelic dysplasia,  Brazilian achondrogenesis,  Grebe chondrodysplasia,  Grebe dysplasia,  Grebe syndrome


  

        

                    


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