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...

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Detalles Bibliográficos
Autores principales: Hariharan, Gopakumar, Ramachandran, Sivji, Parapurath, Rajiv
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Case report
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

Internet

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

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