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Primary Macronodular Adrenal Hyperplasia Associated With Autosomal Dominant ARMC5 Mutation
Background: Primary macronodular adrenal hyperplasia (PMAH) is an uncommon cause of Cushing’s syndrome. In some cases, this is an inherited disorder due to a mutation in the armadillo repeat-containing 5 (ARMC5) gene. Clinical Case: A 43-year-old African American woman presented to clinic with weigh...
Tallennettuna:
| Julkaisussa: | J Endocr Soc |
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| Päätekijät: | , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Oxford University Press
2021
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8089335/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvab048.311 |
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