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Updated: Feb 8, 2026

FISH for Pre-implantation Genetic Diagnosis
Published on: February 23, 2011
Children Born Small for Gestational Age: Differential Diagnosis, Molecular Genetic Evaluation, and Implications
Martijn J J Finken1, Manouk van der Steen2, Carolina C J Smeets2
1Department of Pediatrics, VU University Medical Center, MB Amsterdam, Netherlands.
Insights
Children born small for gestational age (SGA) may face short stature and health risks. Growth hormone (GH) therapy can improve adult height in these children without increasing health risks.
Area of Science:
- Pediatrics
- Endocrinology
- Genetics
Background:
- Small for gestational age (SGA) describes infants with birth weight/length below -2 SD score (SDS).
- Causes of SGA are diverse, including maternal, placental, and fetal factors.
- While most SGA infants achieve catch-up growth, approximately 10% remain short.
Purpose of the Study:
- To review the implications of being born small for gestational age.
- To discuss the efficacy and safety of growth hormone (GH) treatment for short children born SGA.
- To explore potential add-on therapies for optimizing adult height.
Main Methods:
- Literature review of studies on SGA, growth, and treatment outcomes.
- Analysis of short-term and long-term consequences of SGA.
- Evaluation of GH therapy and combined GnRH agonist treatment in SGA populations.
Main Results:
- Short children born SGA benefit from GH treatment, increasing adult height by an average of 1.25 SDS.
- Combined gonadotropin-releasing hormone agonist therapy may be considered for severe cases with predicted adult height below -2.5 SDS.
- GH treatment for SGA does not appear to confer additional health risks.
Conclusions:
- SGA is a heterogeneous condition with potential long-term health implications.
- GH therapy is an effective and safe treatment for improving adult height in short children born SGA.
- Further consideration of combined therapies may be warranted for specific patient subgroups.
Abstract:
Children born small for gestational age (SGA), defined as a birth weight and/or length below -2 SD score (SDS), comprise a heterogeneous group. The causes of SGA are multifactorial and include maternal lifestyle and obstetric factors, placental dysfunction, and numerous fetal (epi)genetic abnormalities. Short-term consequences of SGA include increased risks of hypothermia, polycythemia, and hypoglycemia. Although most SGA infants show catch-up growth by 2 years of age, ∼10% remain short. Short children born SGA are amenable to GH treatment, which increases their adult height by on average 1.25 SD. Add-on treatment with a gonadotropin-releasing hormone agonist may be considered in early pubertal children with an expected adult height below -2.5 SDS. A small birth size increases the risk of later neurodevelopmental problems and cardiometabolic diseases. GH treatment does not pose an additional risk.
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