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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Main Authors: | , , , , , |
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Format: | Article |
Language: | English |
Published: |
Wiley
2016-01-01
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Series: | Case Reports in Surgery |
Online Access: | http://dx.doi.org/10.1155/2016/8605673 |
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