Allelic Variants of ARMC5 in Patients With Adrenal Incidentalomas and in Patients With Cushing's Syndrome Associated With Bilateral Adrenal Nodules

Objective: Germline ARMC5 mutations are considered to be the main genetic cause of primary macronodular adrenal hyperplasia (PMAH). PMAH is associated with high variability of cortisol secretion caused from subclinical hypercortisolism to overt Cushing's syndrome (CS), in general due to bilater...

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Detalles Bibliográficos
Autores principales: Mariani, Beatriz Marinho de Paula, Nishi, Mirian Yumie, Wanichi, Ingrid Quevedo, Brondani, Vania Balderrama, Lacombe, Amanda Meneses Ferreira, Charchar, Helaine, Pereira, Maria Adelaide Albergaria, Srougi, Victor, Tanno, Fabio Yoshiaki, Ceccato, Filippo, Regazzo, Daniela, Barbot, Mattia, Occhi, Gianluca, Albiger, Nora Maria Elvira, Vieira-Corrêa, Marcelo, Kater, Claudio Elias, Scaroni, Carla, Chambô, José Luis, Zerbini, Maria Claudia Nogueira, Mendonca, Berenice B., Almeida, Madson Q., Fragoso, Maria Candida Barisson Villares
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7019100/
https://www.ncbi.nlm.nih.gov/pubmed/32117062
http://dx.doi.org/10.3389/fendo.2020.00036

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7019100/
https://www.ncbi.nlm.nih.gov/pubmed/32117062
http://dx.doi.org/10.3389/fendo.2020.00036

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