Abstract
Factor XIII deficiency is one of the rare clotting factor deficiencies. Although rare, it is an important disorder because of seriousness of its bleeding manifestations, in particular the incidence of intracranial hemorrhage is higher than any other bleeding disorder. Hence an early diagnosis is extremely important where bleeding manifestations can be prevented by prophylactic factor XIII replacement given at every 4-6 week interval. Case1 presents the management of a factor deficiency associated with a very rare blood group AB+ve, while the case 2 reports the successful surgical management with a replacement therapy.
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Poornima, P., Shashibhushan, K., Bharath, K., & Subba Reddy, V. (2010). Factor XIII deficiency: Report of two cases. Journal of Clinical Pediatric Dentistry, 35(1), 101–104. https://doi.org/10.17796/jcpd.35.1.a377042248788418
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