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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Bibliographic Details
Published in: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
Format: Artigo
Language:Inglês
Published: Korean Association of Internal Medicine 1997
Subjects:
Case Report
Online Access: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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