Coexisting Situs Inversus Totalis and Immune Thrombocytopenic Purpura

Situs inversus totalis is a rare congenital abnormality with mirror symmetry of mediastinal and abdominal organs. Immune thrombocytopenic purpura is an autoimmune disease with destruction of thrombocytes. This paper is presentation of surgical approach to a case with coexistence of these two conditi...

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Bibliographic Details
Main Authors: Kemal Gundogdu, Fatih Altintoprak, Mustafa Yener Uzunoğlu, Enis Dikicier, İsmail Zengin, Orhan Yağmurkaya
Format: Article
Language:English
Published: Wiley 2016-01-01
Series:Case Reports in Surgery
Online Access:http://dx.doi.org/10.1155/2016/8605673
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