Growth-Related Characteristics of Patients <18 Years of Age with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency (21OHD): Real World Evidence from the I-CAH Registry

Background: Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (21OHD) is a rare, autosomal recessive disease of the adrenal cortex leading to a lack of cortisol production and compensatory ACTH secretion, which drives excess androgen production. The chronic exposure to excess and...

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Bibliografiset tiedot
Julkaisussa:J Endocr Soc
Päätekijät: Farrar, Mallory, Ali, Salma Rashid, Bryce, Jillian, Baronio, Federico, Claahsen-van der Grinten, Hedi L, Bonfig, Walter, Yonan, Charles, Farber, Robert, Chan, Jean Lin, Ahmed, S Faisal
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Oxford University Press 2021
Aiheet:
Pediatric Endocrinology
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC8090237/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvab048.1457
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