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Published on: June 3, 2016
Obesity, genetics and the skin
1Department of Dermatology, Norfolk and Norwich University Hospitals NHS Foundation Trust, UK. george.millington@nnuh.nhs.uk
Clinical and Experimental Dermatology
|December 21, 2012
Summary
Childhood obesity is a growing public health issue with genetic links. This review focuses on rare monogenic obesity syndromes that often include distinct skin conditions.
Area of Science:
- Pediatric Endocrinology
- Medical Genetics
- Dermatology
Background:
- Childhood obesity presents significant short- and long-term public health challenges.
- Excess body weight is linked to psychological, oncological, metabolic, cardiovascular, musculoskeletal, and dermatological conditions.
- Genetic factors play a role in obesity etiology, including polygenic and monogenic forms.
Purpose of the Study:
- To review monogenic obesity syndromes with a focus on their associated cutaneous (skin) phenotypes.
- To highlight the importance of recognizing syndromic features in obese children.
Main Methods:
- Literature review of monogenic obesity syndromes.
- Analysis of reported cases with specific attention to dermatological manifestations.
- Synthesis of genetic and clinical data.
Main Results:
- Some obese children have monogenic disorders, often presenting with additional syndromic features.
- Certain monogenic obesity syndromes are characterized by distinct cutaneous phenotypes.
- Identifying these syndromes is crucial for accurate diagnosis and management.
Conclusions:
- Monogenic obesity syndromes, particularly those with cutaneous involvement, represent an important area of study.
- Recognition of syndromic features, including skin conditions, aids in diagnosing rare genetic obesity disorders.
- Further research into the genetic and phenotypic spectrum of these syndromes is warranted.
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