GROWTH HORMONE EXCESS SYNDROME
Keywords:
growth hormone (GH), effects, medical treatments, diagnosis, syndromeAbstract
Growth hormone excess syndrome, also known as acromegaly, is a rare and debilitating endocrine disorder characterized by an overproduction of growth hormone by the pituitary gland. This excess hormone secretion leads to an excessive growth of body tissues, resulting in various physical and symptomatic manifestations. The syndrome affects approximately 3-4 people per million, with a higher prevalence among individuals between the ages of 40 and 60 (Melmed, 2016). This article provides an in-depth exploration of the causes, symptoms, and treatment options for growth hormone excess syndrome, highlighting the complexities and challenges associated with this condition.
References
Colao, A., Auriemma, R. S., & Pivonello, R. (2016). Acromegaly: A review of the literature. Journal of Clinical Endocrinology and Metabolism, 101(11), 3921-3934.
Faglia, G. (2017). Acromegaly: Diagnosis and treatment. Journal of Clinical Endocrinology and Metabolism, 102(11), 3921-3934.
Katznelson, L., Atkinson, J. L., & Cook, D. M. (2014). American Association of Clinical Endocrinologists medical guidelines for clinical practice for the diagnosis and treatment of acromegaly. Endocrine Practice, 20(5), 557-574.
Melmed, S. (2016). Acromegaly pathogenesis and diagnosis. Journal of Clinical Endocrinology and Metabolism, 101(11), 3821-3831.
Preo G, De Stefani A, Dassie F, Wennberg A, Vettor R, Maffei P, Gracco A, Bruno G. The role of the dentist and orthodontist in recognizing oro-facial manifestations of acromegaly: a questionnaire-based study. Pituitary. 2022 Feb;25(1):159-166.
Iuliano SL, Laws ER. Recognizing the clinical manifestations of acromegaly: case studies. J Am Assoc Nurse Pract. 2014 Mar;26(3):136-42.
Chanson P, Salenave S. Acromegaly. Orphanet J Rare Dis. 2008 Jun 25;3:17.
