Literature DB >> 1806487

Growth of children with hypochondroplasia treated with growth hormone for up to three years.

N A Bridges1, P C Hindmarsh, C G Brook.   

Abstract

Hypochondroplasia is a skeletal dysplasia characterised by poor childhood growth and an inadequate pubertal growth spurt. 31 children with a radiological diagnosis of hypochondroplasia have been treated for up to 3 years with recombinant human growth hormone, mean dose 17.9 U/m2/week as daily subcutaneous injections. Mean pre-treatment height velocity standard deviation score (SDS) was -0.51; this increased to +1.58 after 1 year of treatment. This improvement diminishes over the next 2 years. The effect on final height remains unknown. There was a considerable variation in clinical response within the group treated.

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Year:  1991        PMID: 1806487     DOI: 10.1159/000182190

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


  1 in total

1.  Hypochondroplasia in a child with 1620C>G (Asn540Lys) mutation in FGFR3.

Authors:  Hüseyin Anıl Korkmaz; Filiz Hazan; Ceyhun Dizdarer; Ajlan Tükün
Journal:  J Clin Res Pediatr Endocrinol       Date:  2012-11-12
  1 in total

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