Lacy's Disease, also known as Lacy's syndrome, is a rare genetic disorder characterized by the presence of distinctive skin lesions and other systemic symptoms. It is caused by mutations in the COL7A1 gene, which plays a crucial role in the formation of collagen, a protein that provides structure to the skin. Individuals with this condition may experience blistering, scarring, and other dermatological issues. The disease is often diagnosed in childhood and can lead to complications such as infections and impaired mobility due to skin damage. Treatment typically focuses on managing symptoms and preventing complications, as there is currently no cure for Lacy's Disease. Regular follow-up with healthcare professionals is essential for affected individuals.