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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...
| Autores principales: | , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2010
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2841604/ https://www.ncbi.nlm.nih.gov/pubmed/20180944 http://dx.doi.org/10.1186/1824-7288-36-1 |