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      Congenital adrenal hyperplasia

      , , ,
      The Lancet
      Elsevier BV

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          Most cited references153

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          Diagnosis and Treatment of Primary Adrenal Insufficiency: An Endocrine Society Clinical Practice Guideline.

          This clinical practice guideline addresses the diagnosis and treatment of primary adrenal insufficiency.
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            Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society* Clinical Practice Guideline

            To update the congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency clinical practice guideline published by the Endocrine Society in 2010.
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              Increased mortality in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

              Reports on mortality in patients with congenital adrenal hyperplasia (CAH) are lacking.

                Author and article information

                Journal
                The Lancet
                The Lancet
                Elsevier BV
                01406736
                January 2023
                January 2023
                : 401
                : 10372
                : 227-244
                Article
                10.1016/S0140-6736(22)01330-7
                36502822
                fd5dfb4f-f0d3-4f5c-8f05-f995d9b90e80
                © 2023

                https://www.elsevier.com/tdm/userlicense/1.0/

                https://doi.org/10.15223/policy-017

                https://doi.org/10.15223/policy-037

                https://doi.org/10.15223/policy-012

                https://doi.org/10.15223/policy-029

                https://doi.org/10.15223/policy-004

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