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Calif Med. 1966 August; 105(2): 104–110.
PMCID: PMC1516352
Achondroplastic Dwarfism—Effects of Treatment with Human Growth Hormone
Roberto F. Escamilla, John J. Hutchings, Choh Hao Li, and Peter Forsham
Abstract
Two male patients with achondroplastic dwarfism aged 7-5/12 and 14½ years were treated with human growth hormone 5 mg daily. Both showed nitrogen retention on balance studies, the older second patient to a marked degree. In the younger patient, height increased from 95.4 to 106.3 cm on hgh 5 mg daily alone for 14 out of 24 months. The rate of growth approximately doubled during the first two treatment periods as compared with the pre-treatment rate. In the second older patient hgh was administered 5 mg daily intramuscularly for 21 out of 33 months. Growth from 129.6 cm to 137.8 cm occurred with the rate increasing following the addition of Na-1-thyroxine to the routine. This increased growth rate occurred during the post-puberty deceleration phase. Bone ages, interpreted from changes in the phalanges and metacarpals, increased from 4½ to 6 years during 16 months in Case 1, and from 13½ to 18 years in 33 months in Case 2. Transient adolescent gynecomastia appeared in Case 2. No local or general toxic effects were noted.
These results are suggestive, but whether or not the eventual height of an achondroplastic dwarf can be significantly altered must await further studies.
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Selected References
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  • ESCAMILLA RF, BENNETT L. Pituitary infantilism treated with purified growth hormone, thyroid, and sublingual methyltestosterone; a case report. J Clin Endocrinol Metab. 1951 Feb;11(2):221–228. [PubMed]
  • ESCAMILLA RF, HUTCHINGS JJ, DEAMER WC, LI CH, FORSHAM PH. Long-term effects of human growth hormone (Li) in a pituitary dwarf. J Clin Endocrinol Metab. 1961 Jun;21:721–726. [PubMed]
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  • HUTCHINGS JJ, ESCAMILLA RF, LI CH, FORSHAM PH. LI HUMAN GROWTH HORMONE ADMINISTRATION IN GONADAL DYSGENESIS. Am J Dis Child. 1965 Apr;109:318–321. [PubMed]
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