Bilateral internal carotid agenesis is a rare congenital malformation, poorly documented in the literature. We report the case of a 5 year old patient with an incidental diagnosis of this entity, after an evaluation of an open craniocerebral trauma and post-traumatic seizures. Patient diagnosis was performed by a magnetic resonance angiography showing no reflux of internal carotid arteries (bilateral agenesis) and an increase in the caliber of vertebral and basilar arteries.
Polet Portillo-Cálix, Alison Miralda-Cálix, Aarón Mejía-Fúnez and Carlos Figueroa-López
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