Alström Syndrome

Alström Syndrome is a rare genetic disorder that affects many parts of the body. It is caused by mutations in a specific gene and is inherited from parents. People with the syndrome often experience vision and hearing loss, develop heart and lung issues, and may have problems with their kidneys, liver, and metabolism. It can also lead to early-onset type 2 diabetes and obesity. The symptoms and severity can vary, and there is no cure. Treatment focuses on managing individual symptoms and preventing complications, requiring a multidisciplinary approach with healthcare providers.