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Factor XIII deficiency in a newborn] |
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| Authors: | R Diehl S Thouvenin J Reynaud K Jamal-Bey G Teyssier J-L Stéphan C Berger |
| Affiliation: | 1. CIC-EC Inserm, CIE3, CHU Hôpital Nord, Saint-Etienne, France;2. Département de Médecine Générale, Faculté Jacques Lisfranc, Université Jean Monnet, Saint-Etienne, France;3. EA3065, Université Jean Monnet, PRES de Lyon, Saint-Etienne, France;4. Service de Médecine Vasculaire et Thérapeutique, CHU de Saint-Etienne, Saint-Etienne, France;5. Service de Médecine Vasculaire, CHU de Caen, Caen, France;6. Hospitalisation Médicale d''Urgences, CHU de Saint-Etienne, Saint-Etienne, France |
| Abstract: | Factor XIII deficiency is an uncommon inherited disorder which is characterized by umbilical cord bleeding and an unusually high incidence of intracranial hemorrhage. We report here a case of Factor XIII deficiency in a child that presented a caput. succedaneum as the first manifestation of the disease and then an umbilical cord bleeding. The importance of performing a quantitative FXIII assay in the presence of strong clinical suspicion is strengthened because of the normality of the standard screening tests and the important therapeutic consequences. |
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