153 top medical experts on Type V Osteogenesis Imperfecta across 13 countries and 4 U.S. states, including 15 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Type V Osteogenesis Imperfecta: A moderate form of osteogenesis imperfecta characterized by increased bone fragility and low bone mass that clinically manifests with susceptibility to bone fractures of variable severity, metaphyseal changes at birth, short stature, dislocation of the radial head, mineralized interosseous membranes, hyperplasic callus (occurring more often during periods of more rapid growth), white sclera and absence of dentinogenesis imperfecta.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Type V OI,  Type 5 type 5 Osteogenesis Imperfecta OI,  Type V type V Osteogenesis Imperfecta OI,  OI5 Osteogenesis Imperfecta 5,  Osteogenesis imperfecta with normal sclerae,  type 5 Osteogenesis imperfecta


  

        

                    


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