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Basilar artery thrombosis in a child heterozygous for factor V Leiden mutation
A Verdú1, M R Cazorla, M A Granados
1Pediatric Neurology Unit, Hospital Virgen de la Salud, Toledo, Spain.
Pediatric Neurology
|February 22, 2001
Abstract:
Activated protein C resistance, usually because of factor V Leiden mutation, is considered to be the most common hereditary prothrombotic condition. A 9-year-old male with a basilar artery stroke and activated protein C resistance is described. The patient, found to be heterozygous for factor V Leiden mutation, is one of several recent reports that suggest that activated protein C resistance is an important risk factor for spontaneous arterial thrombosis in infancy and childhood.