Congenital Hypofibrinogenemia in a Neonate with a Novel Mutation in the <i>FGB</i> Gene

• Главные авторы: Jun Shinozuka (Автор), Nobuo Okumura (Автор), Mayumi Nagasawa (Автор), Motokazu Nishikado (Автор), Sayaka Kadowaki (Автор), Itsuro Katsuda (Автор), Shinsaku Imashuku (Автор)
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• Опубликовано: MDPI AG, 2021-03-01T00:00:00Z.
• Предметы: article
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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...