Carney Complex Explanation of the Condition: Carney Complex, also known as Carney syndrome, is a rare genetic disorder characterized by the development of multiple tumors in various parts of the body, including the heart. It is caused by mutations in the PRKAR1A gene. The condition is typically inherited in an autosomal dominant pattern, meaning that a person with one affected parent has a 50% chance of inheriting the condition. Clinical Features: Carney Complex can present with a wide range of