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A Case of Coagulation Factor V Deficiency Complicated with Intracranial Hemorrhage
Factor V deficiency is a relatively uncommon disorder, inherited as an autosomal recessive trait that manifests clinically only in individuals who inherit the defective gene from both parents. The hemorrhage of nasal and oral cavity and ecchymosis are common but intracranial hemorrhage is very rare....
Uloženo v:
| Vydáno v: | Korean J Intern Med |
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| Hlavní autoři: | , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Korean Association of Internal Medicine
1997
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4531966/ https://ncbi.nlm.nih.gov/pubmed/9159044 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3904/kjim.1997.12.1.80 |
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