Congenital Hypofibrinogenemia in a Neonate with a Novel Mutation in the FGB Gene

Detection of severe hypofibrinogenemia (<50 mg/dL) in a neonate soon after birth is alarming because of the risk of hemorrhage. A female neonate was noted to be hypofibrinogenemic (<50 mg/dL) on day 0 of birth; she showed no thrombocytopenia/coagulopathy or hemorrhagic symptoms. Considering th...

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Detalles Bibliográficos
Autores principales: Shinozuka, Jun, Okumura, Nobuo, Nagasawa, Mayumi, Nishikado, Motokazu, Kadowaki, Sayaka, Katsuda, Itsuro, Imashuku, Shinsaku
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7930968/
https://www.ncbi.nlm.nih.gov/pubmed/33804389
http://dx.doi.org/10.3390/pediatric13010016

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7930968/
https://www.ncbi.nlm.nih.gov/pubmed/33804389
http://dx.doi.org/10.3390/pediatric13010016

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