Abstract
Hypochondroplasia is a cause of disproportionate short stature and characterized by minor clinical manifestations. The aim of this study was to evaluate the efficacy of long-term growth hormone (GH) therapy in hypochondroplastic cases with inadequate response to GH stimulation tests. In this study, six patients who had a height standard deviation score of-3.43 before the treatment and a mean age of 7.42 years and who had received GH treatment at a dose of 0.2 mg/kg/week for a mean period of 4.45 years were evaluated. A good response was found in the first year of treatment, but this increase was not found to be sufficient for the patients to achieve an adequate final height.
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Çetin, T., Şıklar, Z., Kocaay, P., & Berberoğlu, M. (2018). Evaluation of efficacy of long-term growth hormone therapy in patients with hypochondroplasia. JCRPE Journal of Clinical Research in Pediatric Endocrinology, 10(4), 373–376. https://doi.org/10.4274/JCRPE.0043
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