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Released: 2025-05-20

Acromegaly is a rare, chronic, progressive disease characterized by an excess secretion of growth hormone (GH) and increased circulating insulin-like growth factor 1 (IGF-1) concentrations. It is caused, in most cases, by pituitary adenomas that interfere with normal pituitary function. The clinical diagnosis, based on symptoms related to GH excess, is often delayed due to the gradual and subtle nature of the disease. Consequently, patients often have established systemic complications at diagnosis with increased morbidity and premature mortality. Our three acromegaly KOLs will discuss patient cases covering the consequences of a delayed diagnosis including strategies for a proper evaluation to avoid a misdiagnosis, address management strategies that can impact overall patient outcomes, and provide an in-depth look at the latest clinical evidence in the acromegaly treatment landscape.


Upon completion of this activity, participants should be better able to:


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