Abstract
Four young males with chronic renal failure and absent or stagnant puberty were treated with testosterone esters. Endocrine evaluation before therapy showed low plasma follicle stimulating hormone (FSH) levels and relatively high luteinizing hormone (LH). Following therapy skeletal maturation accelerated more than growth velocity, resulting in a lower predicted adult height. In three patients osteoporosis increased or rickets developed. Testosterone therapy was effective in developing sex characteristics, but endogenous pubertal development was not stimulated. Growth velocity was increased, but the effect on growth was more than outweighed by bone age acceleration.
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Abbreviations
- CAPD:
-
continuous ambulatory peritoneal dialysis
- FSH:
-
follicle stimulating hormone
- GH:
-
growth hormone
- IGF-1:
-
insulin-like growth factor-1
- LH:
-
luteinizing hormone
- LHRH:
-
luteinizing hormone releasing hormone
- PRL:
-
prolactin
- SDSBA:
-
standard deviation score for bone age
- SDSCA:
-
standard deviation score for chronological age
- SHBG:
-
sex hormone binding globulin
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Van Steenbergen, M.W., Wit, J.M. & Donckerwolcke, R.A.M.G. Testosterone esters advance skeletal maturation more than growth in short boys with chronic renal failure and delayed puberty. Eur J Pediatr 150, 676–680 (1991). https://doi.org/10.1007/BF02072633
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DOI: https://doi.org/10.1007/BF02072633