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How should we investigate children with growth failure?
1Unité 1141, DHU Protect, service d'endocrinologie diabétologie pédiatrique, centre de référence des maladies endocriniennes de la croissance et du développement, Institut national de la santé et de la recherche médicale (Inserm), université Paris Diderot, Sorbonne Paris Cité, hôpital Robert-Debré, Assistance publique-Hôpitaux de Paris, 48, boulevard Sérurier, 75019 Paris, France.
Early diagnosis of short stature in children is crucial. Investigations differentiate physiological short stature from genetic defects, skeletal dysplasia, or chronic diseases for timely treatment.
Area of Science:
- Pediatrics
- Endocrinology
- Genetics
Background:
- Short stature in children necessitates early and accurate diagnosis for effective management.
- Growth failure can stem from various underlying conditions, requiring comprehensive evaluation.
Purpose of the Study:
- To outline the essential investigations for diagnosing short stature in children.
- To differentiate between physiological variants and pathological causes of growth failure.
Main Methods:
- Review of diagnostic approaches for pediatric short stature.
- Categorization of short stature causes including idiopathic, primary, and secondary deficits.
Main Results:
- Idiopathic short stature includes familial short stature and constitutional delay of growth and puberty.
- Primary causes encompass syndromic/genetic defects and skeletal dysplasia.
- Secondary deficits arise from endocrine disorders, chronic diseases (celiac, Crohn's), malnutrition, or anorexia nervosa.
Conclusions:
- Comprehensive investigation is key to identifying the specific cause of short stature.
- Distinguishing between different etiological categories ensures appropriate therapeutic strategies.
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