| Literature DB >> 34504723 |
Sonali Malhotra1, Ramya Sivasubramanian2, Gitanjali Srivastava3.
Abstract
One in five children and adolescents in the United States are diagnosed with obesity and nearly 6% of them are being classified under the severe obesity category. With over 7% of severe obesity being attributed to genetic disorders, in this review we aim to focus on monogenic and syndromic obesity: its etiology, wide spectrum of clinical presentation, criticalness of early identification, and limited management options. Advanced genetic testing methods including microarray and whole genome sequencing are imperative to identify the spectrum of mutations and develop targeted treatment strategies including personalized multidisciplinary care, use of investigational drugs, and explore surgical options in this unique subset of severe pediatric obesity. Thieme. All rights reserved.Entities:
Keywords: genetic obesity; hyperphagia; infantile obesity; pediatric obesity; pediatric weight management; weight-for-length percentile
Year: 2021 PMID: 34504723 PMCID: PMC8416234 DOI: 10.1055/s-0041-1731035
Source DB: PubMed Journal: J Pediatr Genet ISSN: 2146-460X