Congenital Coagulation Factor XIII Deficiency Revealed by Convulsion: A Case Report
N. Mebrouk, T. Benouachane, L. Chtouki, F. Jabourik & A. Bentahila · Asian Journal of Pediatric Research · 2021
Factor XIII deficiency is a rare inherited disease, with a particularly high risk of intracerebral hemorrhage. We report the case of a newborn who was suspected to have a coagulation disorder at birth, due to an intracerebral hemorrhage. A quantitative dosage of factor XIII was r...
Open access
Research Article
10.9734/ajpr/2021/v6i130187