Recurrent intraparenchymal brain hemorrhage in an infant with factor XIII deficiency

• Asıl Yazarlar: Devdeep Mukherjee (Yazar), Dibyendu De (Yazar), Satyajit Das (Yazar), Gopikrishna Kurasa (Yazar)
• Materyal Türü: Kitap
• Baskı/Yayın Bilgisi: Hygeia Press di Corridori Marinella, 2021-05-01T00:00:00Z.
• Konular: article
• Online Erişim: 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...