41 top medical experts on type 5 congenital Adrenal hyperplasia across 6 countries and 2 U.S. states, including 10 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. type 5 congenital Adrenal hyperplasia: 46,XY disorder of sex development due to isolated 17,20-lyase deficiency is a rare disorder of sex development due to reduced 17,20-lyase activity that affects individuals with 46,XY karyotype and is characterized by ambiguous external genitalia, including micropenis, perineal hypospadias, bifid scrotum, cryptorchidism, and a blind vaginal pouch. Blood pressure and electrolytes are normal whilst hormonal investigations show normal basal and stimulated levels of cortisol, and low basal and stimulated androgen levels.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: 17-alpha-hydroxylase deficiency,  Adrenal Hyperplasia V,  Due To 17-Alpha-Hydroxylase Deficiency Congenital Adrenal Hyperplasia,  congenital due to 17-alpha-hydroxylase deficiency Adrenal hyperplasia


  

        

                    


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