The natural history of 21-hydroxylase autoantibodies in autoimmune Addison’s disease

BACKGROUND: The most common cause of primary adrenal failure (Addison’s disease) in the Western world is autoimmunity characterized by autoantibodies against the steroidogenic enzyme 21-hydroxylase (CYP21A2, 21OH). Detection of 21OH-autoantibodies is currently used for aetiological diagnosis, but ho...

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Salvato in:
Dettagli Bibliografici
Pubblicato in:Eur J Endocrinol
Autori principali: Wolff, Anette Boe, Breivik, Lars, Hufthammer, Karl Ove, Grytaas, Marianne Aardal, Bratland, Eirik, Husebye, Eystein Sverre, Oftedal, Bergithe Eikeland
Natura: Artigo
Lingua:Inglês
Pubblicazione: Bioscientifica Ltd 2021
Soggetti:
Clinical Study
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC8052519/
https://ncbi.nlm.nih.gov/pubmed/34665570
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1530/EJE-20-1268
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