Abstract
RENDU-OSLER's disease is a rare hereditary disease of autosomal dominant transmission, it is a condition characterized by mucocutaneous and visceral telangiectasias; often revealed by recurrent epistaxis, hemostasis can be difficult. We report the observation of a 10-year-old girl who presented with chronic abdominal pain secondary to a subcapsular hematoma of the liver due to the rupture of an arteriovenous malformation falling within the framework of RENDU- OSLER
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