126 top medical experts on Hyperostosis corticalis deformans juvenilis across 14 countries and 3 U.S. states, including 11 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Hyperostosis corticalis deformans juvenilis: Juvenile Paget disease is a very rare form of Paget disease of the bone characterized by a general increase in bone turnover with increased bone resorption and deposition, resulting in cortical and trabecular thickening, and clinically presenting as progressive skeletal deformities, growth impairment, fractures, vertebral collapse, skull enlargement and sensorineural hearing loss.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Support Organizations
  4. Synonyms: Chronic Congenital Idiopathic Hyperphosphatasemia,  Familial Idiopathic Hyperphosphatasemia,  Familial Osteoectasia,  Hyperphosphatasemia with Bone Disease,  chronic congenital idiopathic Hyperphosphatasemia,  familial idiopathic Hyperphosphatasia,  Idiopathic Hyperphosphatasia,  Juvenile Paget Disease,  Juvenile Paget's Disease,  Osteochalasia Desmalis Familiaris,  Osteoectasia with Hyperphosphatasia,  familial Osteoectasia,  juvenile-onset Paget disease of bone 5


  

        

                    


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