Coagulation factor XIII deficiency – Report of a newborn F13A1 Val34Leu polymorphism carrier

Coagulation factor XIII deficiency – Report of a newborn F13A1 Val34Leu polymorphism carrier

Coagulation factor XIII deficiency (FXIIID) is a rare inherited autosomal recessive bleeding disorder. FXIIID is the only coagulation factor deficiency that has been associated with pregnancy loss. Regarding neonates, prolonged umbilical cord bleeding and intracranial hemorrhage, a life-threatening...

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Bibliographic Details
Main Authors: Georgios N. Katsaras, Dimitra Gialamprinou, Ilias Chatziioannidis, Paraskevi Karagianni, Georgios Mitsiakos
Format: Article
Language:English
Published: Hygeia Press di Corridori Marinella 2022-10-01
Series:Journal of Pediatric and Neonatal Individualized Medicine
Subjects:
f13a1 val34leu
polymorphism
recurrent pregnancy loss
prolonged umbilical cord bleeding
intracranial hemorrhage
Online Access:https://jpnim.com/index.php/jpnim/article/view/1174

Internet

https://jpnim.com/index.php/jpnim/article/view/1174

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