Pituitary gigantism treated successfully with the growth hormone receptor antagonist, pegvisomant [Letter]
Description
A Caucasian male aged 15 years presented with 2 years accelerated linear growth. He was 202 cm tall at presentation, with calculated mid-parental height of 173 cm. There were no features of hypopituitarism or acral growth. His visual fields and optic discs were normal...
Impact and interest:
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ID Code: | 94206 | ||
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Item Type: | Contribution to Journal (Letter) | ||
Refereed: | No | ||
ORCID iD: |
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Additional Information: | Letter | ||
Measurements or Duration: | 3 pages | ||
Keywords: | Hormone Antagonists, Human Growth Hormone, Humans, Membrane Proteins, Treatment Outcome, adolescent, androgen therapy, angiopeptin, clinical article, gigantism, growth plate, human, hypophysis adenoma, hypophysis disease, letter, male, nuclear magnetic resonance imaging, pegvisomant, pituitary gigantism, priority journal, somatomedin C | ||
DOI: | 10.1111/imj.12077 | ||
ISSN: | 1445-5994 | ||
Pure ID: | 34522113 | ||
Divisions: | Past > QUT Faculties & Divisions > Faculty of Health Past > Institutes > Institute of Health and Biomedical Innovation |
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Copyright Owner: | Consult author(s) regarding copyright matters | ||
Copyright Statement: | This work is covered by copyright. Unless the document is being made available under a Creative Commons Licence, you must assume that re-use is limited to personal use and that permission from the copyright owner must be obtained for all other uses. If the document is available under a Creative Commons License (or other specified license) then refer to the Licence for details of permitted re-use. It is a condition of access that users recognise and abide by the legal requirements associated with these rights. If you believe that this work infringes copyright please provide details by email to qut.copyright@qut.edu.au | ||
Deposited On: | 29 Mar 2016 00:35 | ||
Last Modified: | 31 Mar 2024 13:44 |
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