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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Detalles Bibliográficos
Autores principales: Gundogdu, Kemal, Altintoprak, Fatih, Uzunoğlu, Mustafa Yener, Dikicier, Enis, Zengin, İsmail, Yağmurkaya, Orhan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4769751/
https://www.ncbi.nlm.nih.gov/pubmed/26981307
http://dx.doi.org/10.1155/2016/8605673

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4769751/
https://www.ncbi.nlm.nih.gov/pubmed/26981307
http://dx.doi.org/10.1155/2016/8605673

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