200 top medical experts on Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency across 22 countries and 5 U.S. states, including 19 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency: A rare form of classic congenital adrenal hyperplasia (CAH) characterized by glucocorticoid deficiency, hyperandrogenism, hypertension and virilization in females.
  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: 11 Beta Hydroxylase Deficiency,  11-Beta-hydroxylase deficiency,  11B Hydroxylase Deficiency,  Adrenal Hyperplasia IV,  Due To Steroid 11-Beta-Hydroxylase Deficiency Congenital Adrenal Hyperplasia,  Hypertensive Form Adrenal Hyperplasia,  Adrenal hyperplasia 4,  due to 11-Beta-hydroxylase deficiency congenital Adrenal hyperplasia,  CYP11B1 deficiency congenital,  Congenital adrenal hyperplasia type 4,  Hypertensive form of adrenal hyperplasia,  Increased urinary 11-deoxytetrahydrocorticosterone level,  P450C11B1 deficiency,  Steroid 11 Beta Hydroxylase Deficiency,  Steroid 11-Beta-Hydroxylase Deficiency,  congenital CYP11B1 deficiency


  

        

                    


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