Bardet-Biedl syndrome is a rare genetic disorder that affects multiple parts of the body. It is characterized by symptoms such as obesity, vision problems, and kidney issues. People with this syndrome may also experience learning difficulties and extra fingers or toes, known as polydactyly. The condition is caused by mutations in specific genes that are important for cell function. Diagnosis of Bardet-Biedl syndrome often involves a combination of clinical evaluation and genetic testing. Treatment focuses on managing symptoms and may include weight management, vision care, and support for learning challenges. Early intervention can help improve the quality of life for those affected by this condition.