Real-World Evidence of Clinical Outcomes in Patients With Assumed Classic Congenital Adrenal Hyperplasia in the United States

Background: Classic congenital adrenal hyperplasia (CAH) is an autosomal recessive disorder, usually due to a deficiency in the 21-hydroxylase enzyme, that results in impaired cortisol synthesis and excess androgen production. Patients with classic CAH experience both disease-related features from e...

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Vydáno v:J Endocr Soc
Hlavní autoři: Farrar, Mallory, Farber, Robert, Sen, Ginny P, Yonan, Charles, Chan, Jean Lin
Médium: Artigo
Jazyk:Inglês
Vydáno: Oxford University Press 2021
Témata:
Adrenal
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC8089243/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvab048.187
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