Clinical Updates on Acromegaly
A special issue of Journal of Clinical Medicine (ISSN 2077-0383). This special issue belongs to the section "Endocrinology & Metabolism".
Deadline for manuscript submissions: 20 February 2026 | Viewed by 3
Special Issue Editors
Interests: acromegaly; insulin-like growth factor; cancer; pituitary ACTH hypersecretion; pituitary adenoma
Special Issues, Collections and Topics in MDPI journals
Interests: acromegaly; vitamin d; osteoporotic fractures in acromegaly patients; endocrinology; primary adrenal insufficiency
Interests: endocrinology; pituitary disease; acromegaly; insulin-like growth factor; pituitary adenoma
Special Issue Information
Dear Colleagues,
This Special Issue aims to compile a collection of articles on the latest and most relevant research directions in the field of acromegaly.
Acromegaly is an endocrine disease mainly caused by growth hormone-secreting pituitary adenoma. Persistent excessive secretion of growth hormone (GH) and its peripheral mediator, insulin-like growth factor-1 (IGF-1), results in numerous complications, including those related to the cardiovascular, respiratory, and musculoskeletal systems.
Personalized diagnostic and therapeutic management is essential in providing care to each patient with acromegaly.
We invite specialists in the field of neuroendocrinology to share their experiences and observations. Original papers and review articles are welcome.
Prof. Dr. Marek Bolanowski
Dr. Jowita Halupczok-Żyła
Prof. Dr. Aleksandra Gilis-Januszewska
Prof. Dr. Przemysław Witek
Guest Editors
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Keywords
- acromegaly
- GH
- IGH-1
- growth hormone-secreting pituitary adenoma
- pituitary adenoma
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