Marfan's syndrome, dextrocardia and situs inversus associated with discrete subaortic stenosis and aortic insufficiency in an adult female: Case report
JOURNAL OF HEART VALVE DISEASE, vol.10, no.3, pp.415-417, 2001 (SCI-Expanded, Scopus)
- Publication Type: Article / Article
- Volume: 10 Issue: 3
- Publication Date: 2001
- Journal Name: JOURNAL OF HEART VALVE DISEASE
- Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
- Page Numbers: pp.415-417
- Karadeniz Technical University Affiliated: Yes
Abstract
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.