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

Otto Westphal
Author Information
  1. Otto Westphal: Queen Silvia Childrens Hospital, The Sahlgrenska Academy, University of Gothenburg, Goteborg, Sweden. otto.westphal@vgregion.se

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.

MeSH Term

Adolescent
Body Height
Child
Child, Preschool
Female
Growth
Human Growth Hormone
Humans
Male
Mutation
Noonan Syndrome
Protein Tyrosine Phosphatase, Non-Receptor Type 11
Puberty

Chemicals

Human Growth Hormone
PTPN11 protein, human
Protein Tyrosine Phosphatase, Non-Receptor Type 11