This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages before signing in

Genetic factors and obesity

Authoring team

  • twin, adoption and family studies have shown that genetic factors can play a role in the pathogenesis of obesity
    • however, while obesity runs in families, a Mendelian inheritance pattern is rarely evident
    • exceptions include uncommon disorders such as:
      • Prader-Willi syndrome (autosomal dominant, 1 in 25,000)
      • Bardet-Biedl syndrome (autosomal recessive, 1 in 100,000) syndromes
      • note that there have also been described monogenic forms of obesity such as congenital leptin deficiency and melanocortin-3 receptor mutations - these monogenic forms account for only a small proportion of cases of morbid obesity

Reference:

  1. Xia Q, Grant SF; The genetics of human obesity. Ann N Y Acad Sci. 2013 Jan 29.

Related pages

Create an account to add page annotations

Add information to this page that would be handy to have on hand during a consultation, such as a web address or phone number. This information will always be displayed when you visit this page