Recurrent intraparenchymal brain hemorrhage in an infant with factor XIII deficiency

• 主要な著者: Devdeep Mukherjee (著者), Dibyendu De (著者), Satyajit Das (著者), Gopikrishna Kurasa (著者)
• フォーマット: 図書
• 出版事項: Hygeia Press di Corridori Marinella, 2021-05-01T00:00:00Z.
• 主題: article
• オンライン･アクセス: Connect to this object online.

Factor XIII deficiency is an autosomal recessive disorder with an incidence of 1 in 1-5 million. On activation factor XIII stabilizes clot formation by cross-linking fibrin strands. Deficiency is characterized by severe bleeding due to impairment in clot formation. We describe a case of a child pres...