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Coexisting Situs Inversus Totalis and Immune Thrombocytopenic Purpura

  • Gundogdu K
  • Altintoprak F
  • Uzunoğlu M
  • et al.
Case Reports in Surgery (2016) 2016 1-3
DOI: 10.1155/2016/8605673
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Abstract

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 conditions.

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Gundogdu, K., Altintoprak, F., Uzunoğlu, M. Y., Dikicier, E., Zengin, İ., & Yağmurkaya, O. (2016). Coexisting Situs Inversus Totalis and Immune Thrombocytopenic Purpura. Case Reports in Surgery, 2016, 1–3. https://doi.org/10.1155/2016/8605673

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