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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:J Endocr Soc
Prif Awduron: Rivera Nazario, Ivan Augusto, Moya, Kyomara Hernandez, Ortiz, Arnaldo Nieves, Rivera, Jose Ayala, Figueroa, Arnaldo Rojas, Cintron-Colon, Hector R, Miranda, Maria De Lourdes
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Oxford University Press 2021
Pynciau:
Neuroendocrinology and Pituitary
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC8090562/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvab048.1186
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