Please use this identifier to cite or link to this item:
https://hdl.handle.net/2440/39610
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Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Court, F. | - |
dc.contributor.author | Wemyss-Holden, S. | - |
dc.contributor.author | Fitridge, R. | - |
dc.contributor.author | Maddern, G. | - |
dc.date.issued | 2003 | - |
dc.identifier.citation | ANZ Journal of Surgery, 2003; 73(9):772-773 | - |
dc.identifier.issn | 1445-1433 | - |
dc.identifier.issn | 1445-2197 | - |
dc.identifier.uri | http://hdl.handle.net/2440/39610 | - |
dc.description | The definitive version is available at www.blackwell-synergy.com | - |
dc.description.abstract | Morgagni herniae are rare congenital diaphragmatic hernia, which normally present late in adult life with minimal symptoms. They are always associated with a peritoneal hernial sac, and often contain transverse colon or stomach. We present an unusual case of a Morgagni hernia containing caecum in an 81-year-old woman, post ruptured aortic aneurysm repair. | - |
dc.language.iso | en | - |
dc.publisher | Blackwell Science Asia | - |
dc.source.uri | http://dx.doi.org/10.1046/j.1445-2197.2003.02745.x | - |
dc.subject | Malrotation | - |
dc.subject | Woman | - |
dc.subject | Adult | - |
dc.subject | Diaphragmatic hernia | - |
dc.title | Unusual case of Morgagni hernia associated with malrotation | - |
dc.type | Journal article | - |
dc.identifier.doi | 10.1046/j.1445-2197.2003.02745.x | - |
pubs.publication-status | Published | - |
dc.identifier.orcid | Fitridge, R. [0000-0001-6258-5997] | - |
dc.identifier.orcid | Maddern, G. [0000-0003-2064-181X] | - |
Appears in Collections: | Aurora harvest 6 Surgery publications |
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