Literature DB >> 20029236

Growth hormone therapy in Noonan syndrome: growth response and characteristics.

Otto Westphal1.   

Abstract

Growth hormone treatment in Noonan syndrome increases growth velocity significantly during the first 2 years of treatment and, to some extent, until puberty. This increase is more pronounced if treatment is started at an early age. Treatment before the age of 5 years is not recommended due to an increased risk of malignancies. In contrast to other growth hormone-treated patients, a slight but significant further increase in height gain can be expected during pubertal growth (at least in boys). Final height improvement varies between 1 and 2 SDS in different studies. Cardiac function does not seem to be impaired during treatment. No significant adverse events have been reported. 2009 S. Karger AG, Basel.

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Year:  2009        PMID: 20029236     DOI: 10.1159/000243778

Source DB:  PubMed          Journal:  Horm Res        ISSN: 0301-0163


  1 in total

Review 1.  Syndromic disorders with short stature.

Authors:  Zeynep Şıklar; Merih Berberoğlu
Journal:  J Clin Res Pediatr Endocrinol       Date:  2014
  1 in total

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