Practical tools to identify short children born small-for-gestational-age eligible for rhGH treatment according to

Gianluca Tornese1, Flavia Pricci2, Maria Chiara Pellegrin3

  • 1Institute for Maternal and Child Health IRCCS "Burlo Garofolo", Trieste, Italy. gianluca.tornese@burlo.trieste.it.

Insights

Many children born small for gestational age (SGA) are eligible for recombinant human growth hormone (rhGH) therapy but remain underdiagnosed. This article offers tools to improve identification and treatment for these short children.

Area of Science:

  • Pediatrics
  • Endocrinology
  • Genetics

Background:

  • Recombinant human growth hormone (rhGH) is a proven therapy for children born small for gestational age (SGA).
  • Despite a prevalence of 1:1800, children treated for SGA are significantly underrepresented compared to those with growth hormone deficiency (GHD).
  • Current data indicates a low treatment prevalence for SGA (0.37/100,000), suggesting underdiagnosis.

Discussion:

  • Many short children born SGA are not identified or are misdiagnosed as GHD, missing crucial rhGH treatment opportunities.
  • The discrepancy highlights a gap in clinical recognition and diagnostic pathways for SGA-related short stature.
  • This underdiagnosis can lead to suboptimal growth outcomes for eligible children.

Key Insights:

  • Underdiagnosis of SGA in short children is a significant issue, leading to missed rhGH treatment.
  • The prevalence of SGA eligible for treatment is considerably higher than current treatment rates suggest.
  • Accurate identification is crucial to ensure children receive appropriate growth-promoting therapies.

Outlook:

  • Development of practical diagnostic tools is essential for better identification of SGA children.
  • Increased awareness and targeted screening can improve rhGH treatment rates for SGA.
  • Future research should focus on optimizing rhGH treatment protocols and long-term outcomes for SGA individuals.

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