Literature DB >> 3132796

The 24-hour growth hormone secretion in a boy with giantism.

P C Hindmarsh1, P J Pringle, C G Brook.   

Abstract

The endocrinological and radiological findings in a 7.5-year-old boy with giantism are reported and compared with an age and sex matched normal tall boy. A 24-h GH profile demonstrated a persistently elevated GH concentration (mean GH concentration: giant 19.3 mU/l; tall boy 5.4 mU/l) with loss of the dominant GH periodicity of 3 h seen in the boy with tall stature and substitution with one of 8 h. These data support the view that giantism and acromegaly are similar diseases occurring prior to and following epiphyseal fusion, respectively.

Entities:  

Mesh:

Substances:

Year:  1988        PMID: 3132796     DOI: 10.1530/acta.0.1170403

Source DB:  PubMed          Journal:  Acta Endocrinol (Copenh)        ISSN: 0001-5598


  2 in total

1.  Pituitary gigantism.

Authors:  P W Lu; M Silink; I Johnston; C T Cowell; M Jimenez
Journal:  Arch Dis Child       Date:  1992-08       Impact factor: 3.791

2.  Intermittent versus continuous administration of growth hormone treatment.

Authors:  V Hakeem; P C Hindmarsh; C G Brook
Journal:  Arch Dis Child       Date:  1993-06       Impact factor: 3.791

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.