Marfan's syndrome, dextrocardia and situs inversus associated with discrete subaortic stenosis and aortic insufficiency in an adult female: Case report

Gokce M., Erdol C., Celik S., Baykan M., Erdol H., Sari A., ...Daha Fazla

JOURNAL OF HEART VALVE DISEASE, cilt.10, sa.3, ss.415-417, 2001 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 10 Sayı: 3
  • Basım Tarihi: 2001
  • Dergi Adı: JOURNAL OF HEART VALVE DISEASE
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.415-417
  • Karadeniz Teknik Üniversitesi Adresli: Evet

Özet

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.