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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Опубликовано в: :Korean J Intern Med
Главные авторы: Yoon, Suk-Gu, Cho, Sung-Tae, Park, Sung-Kyu, Won, Jong-Ho, Baick, Seung-Ho, Hong, Dae-Sik, Park, Hee-Sook
Формат: Artigo
Язык:Inglês
Опубликовано: Korean Association of Internal Medicine 1997
Предметы:
Case Report
Online-ссылка: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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