Coexisting Situs Inversus Totalis and Immune Thrombocytopenic Purpura
Joint Authors
Gundogdu, Kemal
Uzunoğlu, Mustafa Yener
Zengin, İsmail
Yağmurkaya, Orhan
Altintoprak, Fatih
Dikicier, Enis
Source
Issue
Vol. 2016, Issue 2016 (31 Dec. 2016), pp.1-3, 3 p.
Publisher
Hindawi Publishing Corporation
Publication Date
2016-02-14
Country of Publication
Egypt
No. of Pages
3
Main Subjects
Abstract EN
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.
American Psychological Association (APA)
Gundogdu, Kemal& Altintoprak, Fatih& Uzunoğlu, Mustafa Yener& Dikicier, Enis& Zengin, İsmail& Yağmurkaya, Orhan. 2016. Coexisting Situs Inversus Totalis and Immune Thrombocytopenic Purpura. Case Reports in Surgery،Vol. 2016, no. 2016, pp.1-3.
https://search.emarefa.net/detail/BIM-1102896
Modern Language Association (MLA)
Gundogdu, Kemal…[et al.]. Coexisting Situs Inversus Totalis and Immune Thrombocytopenic Purpura. Case Reports in Surgery No. 2016 (2016), pp.1-3.
https://search.emarefa.net/detail/BIM-1102896
American Medical Association (AMA)
Gundogdu, Kemal& Altintoprak, Fatih& Uzunoğlu, Mustafa Yener& Dikicier, Enis& Zengin, İsmail& Yağmurkaya, Orhan. Coexisting Situs Inversus Totalis and Immune Thrombocytopenic Purpura. Case Reports in Surgery. 2016. Vol. 2016, no. 2016, pp.1-3.
https://search.emarefa.net/detail/BIM-1102896
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references
Record ID
BIM-1102896
