Giganto-acromegaly with Hypogonadotrophic Hypogonadism

Authors

  • Mirza Azizul Hoque Endocrinology, Dhaka Medical College, Dhaka
  • Md Bakhtiar Azam (Medicine Unit- Orange, Dhaka Medical College Hospital, Dhaka
  • Md Golam Kibria Khan Medicine, Dhaka Medical College, Dhaka
  • Md Azharul Hoque Neurology, Dhaka Medical College, Dhaka
  • Quazi Deen Mohammad Department of Neurology, Dhaka Medical College. Principal, Dhaka Medical College

DOI:

https://doi.org/10.3329/jom.v10i1.1999

Keywords:

Giganto-acromegaly, hypogonadotrophic hypogonadism

Abstract

Gigantism came from Greek word âGiant'. Pathologically, this condition results from the actions of excessive growth hormone (GH) secretion from the pituitary gland during childhood and adolescent before the closure of epiphyseal growth plates. When the height of an individual is several standard deviations above the mean value for the same age, sex, and ethnicity, the condition is known as gigantism. Pituitary gigantism is extremely rare. If hypersecretion of growth hormone occurs after closure of epiphyseal growth plates the resulting condition is acromegaly. Most patients with gigantism also have features of acromegaly.  

doi:10.3329/jom.v10i1.1999

J Medicine 2009; 10: 22-24

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How to Cite

Hoque, M. A., Azam, M. B., Khan, M. G. K., Hoque, M. A., & Mohammad, Q. D. (2009). Giganto-acromegaly with Hypogonadotrophic Hypogonadism. Journal of Medicine, 10(1), 22–24. https://doi.org/10.3329/jom.v10i1.1999

Issue

Vol. 10 No. 1 (2009)

Section

Case Reports

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