Cowden syndrome

Cowden syndrome is a rare genetic condition that increases the risk of developing multiple benign (non-cancerous) growths called hamartomas, as well as certain cancers, especially of the breast, thyroid, and endometrium. It is caused by mutations in a gene that helps regulate cell growth and division. People with this syndrome may also experience skin changes, such as warty lesions, and have a family history of related health issues. Early detection and regular medical screenings are important to manage health risks associated with Cowden syndrome.