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Congenital Afibrinogenemia presenting as antenatal intracranial bleed: a case report
Congenital afibrinogenemia is a very rare inherited coagulation disorder, characterized by virtual absence of plasma fibrinogen (factor I). There are only about 250 cases reported in the world literature [1]. We describe a case of congenital afibrinogenemia which presented as an antenatally detected...
में बचाया:
| मुख्य लेखकों: | , , |
|---|---|
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
BioMed Central
2010
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2841604/ https://ncbi.nlm.nih.gov/pubmed/20180944 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1824-7288-36-1 |
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