Abstract
A plethora of negative long-term outcomes have been associated with congenital adrenal hyperplasia (CAH). The causes are multiple and involve supra-physiological gluco- and mineralocorticoid replacement, excess adrenal androgens both intrauterine and postnatal, elevated steroid precursor and adrenocorticotropic hormone levels, living with a congenital condition as well as the proximity of the cytochrome P450 family 21 subfamily A member 2 (CYP21A2) gene to other genes. This review aims to discuss the different long-term outcomes of CAH.
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Nordenström, A., Lajic, S., & Falhammar, H. (2022, August 1). Long-Term Outcomes of Congenital Adrenal Hyperplasia. Endocrinology and Metabolism. Korean Endocrine Society. https://doi.org/10.3803/EnM.2022.1528
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