Congenital Hypofibrinogenemia in a Neonate with a Novel Mutation in the <i>FGB</i> 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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| Main Authors: | , , , , , , |
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| Format: | Book |
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MDPI AG,
2021-03-01T00:00:00Z.
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