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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Detalles Bibliográficos
Autores principales: Yoon, Suk-Gu, Cho, Sung-Tae, Park, Sung-Kyu, Won, Jong-Ho, Baick, Seung-Ho, Hong, Dae-Sik, Park, Hee-Sook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Association of Internal Medicine 1997
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4531966/
https://www.ncbi.nlm.nih.gov/pubmed/9159044
http://dx.doi.org/10.3904/kjim.1997.12.1.80

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4531966/
https://www.ncbi.nlm.nih.gov/pubmed/9159044
http://dx.doi.org/10.3904/kjim.1997.12.1.80

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