286 top medical experts on 46,XY Gonadal Dysgenesis across 52 countries and 16 U.S. states, including 120 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. 46,XY Gonadal Dysgenesis: Defects in the SEX determination process in 46, XY individuals that result in abnormal gonadal development and deficiencies in testosterone and subsequently antimullerian hormone or other factors required for normal male sex development. This leads to the development of female phenotypes (male to female sex reversal), normal to tall stature, and bilateral streak or dysgenic gonads which are susceptible to gonadal tissue neoplasms. An XY gonadal dysgenesis is associated with structural abnormalities on the Y chromosome, a mutation in the gene, SRY, or a mutation in other autosomal genes that are involved in sex determination.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): 46,XY Disorder of Sex Development (1,750), Gonadal Dysgenesis (673) and Narrower Categories: Gonadoblastoma (427).
  4. Synonyms: Swyer Syndrome


  

        

                    


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