Basal Cell Carcinoma Syndrome (BCCS) is a genetic condition that increases the risk of developing multiple basal cell carcinomas, a common type of skin cancer. This syndrome is often caused by mutations in the PTCH1 gene, which plays a crucial role in cell growth and division. Individuals with BCCS may also experience other abnormalities, such as jaw cysts and skeletal malformations. People with BCCS typically develop skin lesions at a younger age than the general population. Regular skin examinations and protective measures, such as using sunscreen, are essential for managing the risk of skin cancer. Early detection and treatment can help prevent complications associated with this syndrome.