314 top medical experts on Congenital adrenal hyperplasia due to 21 hydroxylase deficiency across 53 countries and 17 U.S. states, including 150 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 21 hydroxylase deficiency: A form of congenital adrenal hyperplasia (CAH) characterized by simple virilizing or salt wasting forms that can manifest with abnormal genital development with variable levels of virilization in females and with adrenal insufficiency in both sexes, and that presents with dehydration and hypoglycemia (which can be lethal if left untreated) in the neonatal period, as well as hyperandrogenia.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: 21 alpha hydroxylase deficiency,  21 hydroxylase deficiency,  21-Hydroxylase Deficiency,  Adrenal hyperplasia III,  Attenuated congenital adrenal hyperplasia,  CYP21 deficiency,  Congenital adrenal hyperplasia 1,  LOCAH,  Late-onset congenital adrenal hyperplasia,  NCCAH,  Non classic congenital adrenal hyperplasia


  

        

                    


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