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Published in 2022 at "Frontiers in Endocrinology"
DOI: 10.3389/fendo.2022.1005963
Abstract: Background Classic congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is a rare autosomal recessive condition characterized by cortisol deficiency and excess androgen production. The current standard of care is glucocorticoid (GC) therapy, and sometimes…
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Keywords:
consensus;
adults classic;
classic congenital;
unmet needs ... See more keywords