Marfan’s Syndrome, Dextrocardia and Situs Inversus Associated with Discrete Subaortic Stenosis and Aortic Insufficiency in an Adult Female: Case Report
Mustafa Gökçe MD, Cevdet Erdöl MD, Sükrü Çelik MD, Merih Baykan MD, Hidayet Erdöl MD, Ahmet Sari MD, Ali Ahmetoglu MD

Marfan’s syndrome is an inherited connective tissue defect that affects many organs, especially of the musculoskeletal, ophthalmic and cardiovascular systems, and may be associated with some rare conditions. Here, we report the first known case of Marfan’s syndrome, combined with situs inversus totalis with dextrocardia and discrete subaortic stenosis and aortic insufficiency in a 22-year-old woman.