Maffucci Syndrome is a rare genetic disorder characterized by the presence of multiple enchondromas, which are benign bone tumors, and hemangiomas, which are abnormal blood vessel formations. These tumors typically develop in the bones and soft tissues, leading to potential complications such as fractures and deformities. The exact cause of Maffucci Syndrome is not fully understood, but it is believed to be linked to mutations in the IDH1 or IDH2 genes. Individuals with this syndrome may require regular monitoring and treatment to manage symptoms and prevent complications associated with the tumors.