Marfan syndrome is a genetic disorder that affects connective tissue, causing abnormal growth and development. It is inherited in an autosomal dominant pattern due to a mutation in the FBN1 gene on chromosome 15. If one parent has Marfan syndrome, a child has a 50% chance of inheriting the condition. While there is no cure, treatment options can help manage symptoms and prevent complications.

1. By: Carson Shaulis