Diagnosis of a Rare Case of Acromegaly Secondary to Pituitary Macroadenoma Debuting as Sudden DKA

Acromegaly is an uncommon clinical syndrome that results from excessive secretion of growth hormone with an annual incidence of 6 to 8 cases per 1 million of individuals with a mean age of diagnosis between 40-45 years. Pituitary adenomas can be the principal reason for an overgrowth of the anterior...

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Detalles Bibliográficos
Autores principales: Rivera Nazario, Ivan Augusto, Moya, Kyomara Hernandez, Ortiz, Arnaldo Nieves, Rivera, Jose Ayala, Figueroa, Arnaldo Rojas, Cintron-Colon, Hector R, Miranda, Maria De Lourdes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Neuroendocrinology and Pituitary
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8090562/
http://dx.doi.org/10.1210/jendso/bvab048.1186

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8090562/
http://dx.doi.org/10.1210/jendso/bvab048.1186

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