203 top medical experts on Hyperparathyroidism 2 across 18 countries and 10 U.S. states, including 34 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Hyperparathyroidism 2: A rare genetic disease characterized by synchronous or metachronous occurrence of primary hyperparathyroidism and ossifying fibroma of the maxilla and/or mandible, associated with an increased risk of parathyroid carcinoma. Occurrence of renal cysts or tumors, multiple uterine polyps, and thyroid tumors has also been reported.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Familial Cystic Parathyroid Adenomatosis,  Familial Primary Hyperparathyroidism with Multiple Ossifying Jaw Fibromas,  Hereditary Hyperparathyroidism-Jaw Tumor Syndrome,  Hpt-Jt,  with Multiple Ossifying Jaw Fibromas Familial Primary Hyperparathyroidism,  Hyperparathyroidism-Jaw Tumor Syndrome,  Hereditary Hyperparathyroidism-Jaw Tumor Syndrome


  

        

                    


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