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- Title
Apert Sendromu ve Atriyal Septal Defekt Birlikteliği.
- Authors
Dervişoğlu, Pınar; Kösecik, Mustafa; Kumbasar, Serkan; Salman, Süleyman; Şık, Bulat Aytek; Erdem, Baki; Tekin, Bülent
- Abstract
Apert syndrome, craniosynostosis, mid-face hypoplasia, symmetric syndactyly of the hands and feet, and varying degrees of mental retardation, and is characterized by congenital heart defects. Although the mode of inheritance is autosomal dominant, it creates new mutations in the majority of cases. In this study, an atrial septal defect cases of Apert syndrome, concomitant potential for congenital heart defects, in order to emphasize further investigation, we were willing to offer.
- Publication
Journal of Academic Research in Medicine, 2016, Vol 6, Issue 2, p7
- ISSN
2146-6505
- Publication type
Article
- DOI
10.5152/jarem.2016.896