Genetic Obesity in Children: Overview of Possible Diagnoses with a Focus on SH2B1 Deletion.

Hormone research in paediatrics(2022)

引用 1|浏览14
暂无评分
摘要
Chromosomal microdeletions in 16p11.2, including the SH2B1 gene, in children are associated with severe, early-onset obesity and comorbidities associated with insulin resistance. Early genetic testing in suspicious patients and early screening for comorbidities are recommended.
更多
查看译文
关键词
Body mass index,Insulin resistance,Leptin,Obesity
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要