Source:http://linkedlifedata.com/resource/pubmed/id/15338339
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
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pubmed:dateCreated |
2004-10-25
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pubmed:abstractText |
Non-traumatic spinal epidural haematoma is a rare complication of haemophilia. We report a seven-month-old boy who presented with symptomatic spinal epidural haematoma. He was found to have a hemophilia B trait, and after factor IX replacement, his neurological signs were stabilized and follow-up MRI demonstrated rapid resolution of the haematoma. This illustrative case suggests that surgical intervention can be deferred as the first step in treating spinal epidural haematoma in a haemophilic infant.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0001-6268
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
146
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1263-5
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pubmed:dateRevised |
2009-11-11
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pubmed:meshHeading | |
pubmed:year |
2004
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pubmed:articleTitle |
Resolution of spinal epidural haematoma without surgery in a haemophilic infant.
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pubmed:affiliation |
Department of Neurosurgery, Faculty of Medicine, University of Tokyo, Tokyo, Japan.
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pubmed:publicationType |
Journal Article,
Review,
Case Reports
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