Marfan Sendromu ile Kombine Situs İnversus Totalis Marfan’s Syndrome Combined with Situs Inversus Totalis

  • Editöre Mektup Özet
  • Published 2015

Abstract

Gökçe et al. (1) described the first case of Marfan’s Syndrome (MFS) together with situs inversus totalis (SIT) in 2001. Here we describe the second case. MFS is a well-defined autosomal dominant inherited connective tissue disorder. It has an estimated frequency of 1/5000. MFS is caused by mutation in fibrillin gene (FBN1) located on chromosome 15q21… (More)

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Cite this paper

@inproceedings{zet2015MarfanSI, title={Marfan Sendromu ile Kombine Situs İnversus Totalis Marfan’s Syndrome Combined with Situs Inversus Totalis}, author={Edit{\"{o}re Mektup {\"{O}zet}, year={2015} }