Increased Risk of Autoimmune Disorders in 21-Hydroxylase Deficiency: A Swedish Population-Based National Cohort Study

CONTEXT: The prevalence of autoimmune disorders in individuals with 21-hydroxylase deficiency (21OHD) is unclear. The gene responsible, CYP21A2, is located in a highly immunologically active region. OBJECTIVE: To study the prevalence of autoimmune disorders in individuals with 21OHD. DESIGN, SETTING...

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Bibliografiset tiedot
Julkaisussa:J Endocr Soc
Päätekijät: Falhammar, Henrik, Frisén, Louise, Hirschberg, Angelica Linden, Nordenskjöld, Agneta, Almqvist, Catarina, Nordenström, Anna
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Endocrine Society 2019
Aiheet:
Clinical Research Articles
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6497917/
https://ncbi.nlm.nih.gov/pubmed/31065621
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/js.2019-00122
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