253 top medical experts on Kallmann Syndrome across 34 countries and 18 U.S. states, including 89 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Kallmann Syndrome: A genetically heterogeneous disorder caused by hypothalamic gnrh deficiency and olfactory nerve defects. It is characterized by congenital hypogonadotropic hypogonadism and anosmia, possibly with additional midline defects. It can be transmitted as an X-linked (genetic diseases, X-linked), an autosomal dominant, or an autosomal recessive trait.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Inborn Genetic Diseases (2,477), 46,XY Disorder of Sex Development (1,750), Hypogonadism (2,153).
  4. Clinical Trials ClinicalTrials.gov : at least 18 including 1 Active, 6 Completed, 5 Recruiting


  

        

                    


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