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Research Article Open access CC BY 4.0

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 · pp. 26–29 · Published 15 Jul 2021

10.9734/ajpr/2021/v6i130187

Abstract

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 requested but the usual coagulation tests (thromboplastin, thrombokinase, fibrinogen) were normal.  Because of unavailability of specific treatment with factor XIII concentrate, the patient was treated with fresh frozen plasma.  The initial dose was for normalizing factor XIII; subsequent monthly doses were designed for preventing the occurrence of serious bleeding.

Intracerebral haemorrhage factor XIII fresh frozen plasma pediatrics

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