Final answer:
Marfan syndrome symptoms can vary and include long limbs and fingers, scoliosis, chest deformities, eye issues, and cardiovascular problems, with severity differing among individuals.
Step-by-step explanation:
The symptoms associated with Marfan syndrome can vary significantly among individuals. Marfan syndrome is a genetic disease characterized by defects in fibrillin, which can result in a variety of symptoms. Some common symptoms include long limbs and fingers, scoliosis, chest deformities, eye lens dislocation, and heart problems such as aortic enlargement.
Not all patients with Marfan syndrome display all the symptoms, as it can affect patients differently depending on the severity and presence of the genetic mutation. Medical professionals can use diagnostic tests, such as genetic testing or echocardiograms, to diagnose the presence of Marfan syndrome. It's important to note that Marfan syndrome is inherited in an autosomal dominant pattern, meaning each child of a parent with Marfan syndrome has a 50% chance of inheriting the disorder, regardless of gender.