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Factor V Deficiency Associated with Congenital Cardiac Disorder and Intracranial Hemorrage
Factor V deficiency is an inherited disorder, in which the clotting factor V is low. The disorder is very rare, occurring in only one in one million people. It is inherited as an autosomal recessive disorder. The results of coagulation studies include a prolonged prothrombin time and partial thrombo...
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| Päätekijät: | , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Springer-Verlag
2012
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3636347/ https://ncbi.nlm.nih.gov/pubmed/24426348 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12288-012-0149-8 |
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