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Updated: Aug 9, 2025

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Multidisciplinary Approach to Obesity Management: A Case Report
Published on: May 30, 2025
259
[Obesity in infancy: new precision treatment]
Inge Ruiz1, Thérèse Bouthors1, Sylvie Borloz1
1Unité d'endocrinologie, diabétologie et obésité pédiatrique, Service de pédiatrie, Département femme-mère-enfant, Centre hospitalier universitaire vaudois, 1011 Lausanne.
Revue Medicale Suisse
|February 23, 2023
Summary
Childhood obesity affects 4% of Swiss youth and requires early intervention to prevent adult complications. Genetic testing can identify specific causes, enabling targeted treatments like leptin or setmelanotide for monogenic obesity.
Area of Science:
- Pediatrics
- Endocrinology
- Genetics
Context:
- Childhood obesity is a chronic disease with significant short- and long-term health consequences.
- Approximately 4% of children and adolescents in Switzerland are affected by obesity.
- Early diagnosis and intervention are crucial to prevent the persistence of obesity into adulthood.
Purpose:
- To highlight the importance of prompt diagnosis and multicomponent lifestyle interventions for childhood obesity.
- To emphasize the role of growth and BMI charts in diagnosing obesity and its etiology.
- To discuss the suspicion and molecular diagnosis of monogenic obesity and its targeted therapies.
Summary:
- Growth and BMI charts are essential for diagnosing obesity and identifying its cause in children.
- Severe, early-onset obesity with hyperphagia suggests monogenic obesity, requiring molecular diagnosis.
- Specific genetic defects (LEP, LEPR, POMC, PCSK1) allow for targeted treatments such as leptin or setmelanotide.
Impact:
- Early identification and intervention can mitigate the long-term health impacts of childhood obesity.
- Molecular diagnosis of monogenic obesity opens avenues for personalized and effective therapeutic strategies.
- Understanding the genetic basis of obesity can lead to improved patient outcomes and management protocols.
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