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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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| Publicado no: | Case Rep Surg |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Hindawi Publishing Corporation
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4769751/ https://ncbi.nlm.nih.gov/pubmed/26981307 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2016/8605673 |
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