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[Growth hormone treatment of short children born small for gestational age]
Henrik B Thybo Christesen1, Rikke Bodin Beck Jensen, Niels H Birkebaek
1Odense Universitetshospital, Børneafdelingen, H:S Rigshospitalet, Afdeling for Vaekst.
Insights
Children born small for gestational age (SGA) who remain short may benefit from growth hormone (GH) treatment. This therapy can significantly improve final height in these children.
Area of Science:
- Pediatrics
- Endocrinology
- Growth Disorders
Context:
- Small for gestational age (SGA) is defined by birth weight below -2 SD for gestational age.
- Short SGA children exhibit reduced height (< -2.5 SD) by four years of age.
- Growth hormone (GH) therapy is an approved indication in Europe since 2003 for persistent SGA short stature.
Purpose:
- To describe the Danish consensus guidelines for the diagnosis, treatment, and control of short children born small for gestational age (SGA).
Summary:
- Short children born small for gestational age (SGA) are identified by specific birth weight and childhood height parameters.
- Growth hormone (GH) treatment demonstrates significant efficacy, improving final height by an average of 12 centimeters in SGA children.
- The review outlines established protocols for managing short SGA children.
Impact:
- Provides a framework for consistent and effective management of short SGA children in Denmark.
- Highlights the therapeutic benefits of GH treatment for improving final height outcomes.
- Contributes to the understanding and clinical application of guidelines for SGA short stature.
Abstract:
Short children born small for gestational age (SGA) are defined as having a birth weight below -2 SD for gestational age and a reduced height at four years of age (height < -2.5 SD). Growth hormone (GH) treatment significantly improves final height (mean height gain 12 centimetres) in such children. Consequently, GH therapy has been an approved indication in Europe since 2003 for SGA children who remain short at four years of age. The Danish consensus guidelines for diagnosis, treatment and control of short SGA children are described in this review.
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