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

• 主要な著者: Jun Shinozuka (著者), Nobuo Okumura (著者), Mayumi Nagasawa (著者), Motokazu Nishikado (著者), Sayaka Kadowaki (著者), Itsuro Katsuda (著者), Shinsaku Imashuku (著者)
• フォーマット: 図書
• 出版事項: MDPI AG, 2021-03-01T00:00:00Z.
• 主題: article
• オンライン･アクセス: Connect to this object online.

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...