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Should recombinant human growth hormone therapy be used in short small for gestational age children?
1Paediatric Endocrine Section, Department of Endocrinology, William Harvey Research Institute, Barts and the London Queen Mary School of Medicine, London, UK. l.b.Johnston@qmul.ac.uk
Insights
Short small for gestational age (SGA) children often have short stature. Recombinant human growth hormone (GH) is now approved for treating these children, offering a new therapeutic option.
Area of Science:
- Pediatrics
- Endocrinology
- Growth Disorders
Background:
- Short small for gestational age (SGA) children comprise 20% of pediatric short stature cases.
- SGA short stature presents a significant clinical challenge in growth clinics.
- Limited therapeutic options historically existed for SGA short stature.
Purpose of the Study:
- To examine the role of recombinant human growth hormone (GH) therapy in children born small for gestational age (SGA) who exhibit short stature.
- To review patient selection criteria for GH therapy in this population.
- To assess the effectiveness, safety, and metabolic implications of GH treatment in short SGA children.
Main Methods:
- Review of current literature and clinical guidelines.
- Analysis of data regarding GH therapy outcomes in SGA children.
- Evaluation of safety profiles and potential metabolic side effects.
Main Results:
- Recombinant human growth hormone (GH) is now a licensed treatment for short stature in SGA children in the European Union.
- GH therapy has demonstrated effectiveness in improving growth in short SGA children.
- Safety and metabolic profiles require careful monitoring during treatment.
Conclusions:
- GH therapy represents a significant advancement for managing short stature in SGA children.
- Careful patient selection and monitoring are crucial for optimizing outcomes and safety.
- Further research into long-term metabolic effects is warranted.
Abstract:
Short small for gestational age (SGA) children represent 20% of all children with short stature and therefore constitute a significant portion of the caseload in a growth clinic. The recent approval of recombinant human growth hormone (GH) for the treatment of short stature in SGA children by the European Union's Committee on Proprietary Medicinal Products offers a new licensed therapeutic option. This article examines the role of GH therapy in short SGA children with particular reference to selection of patients, effectiveness, safety, and its potential metabolic implications.
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