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....

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Detalhes bibliográficos
Publicado no:Korean J Intern Med
Main Authors: Yoon, Suk-Gu, Cho, Sung-Tae, Park, Sung-Kyu, Won, Jong-Ho, Baick, Seung-Ho, Hong, Dae-Sik, Park, Hee-Sook
Formato: Artigo
Idioma:Inglês
Publicado em: Korean Association of Internal Medicine 1997
Assuntos:
Case Report
Acesso em linha: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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