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Maheshwari Nallur Siddaraju

Kaiser Permanente, USA

Title: An eight-year-old child with Sneddon syndrome: A rare case report

Abstract

We present a rare case of slow-progressing neurocutaneous vasculopathy described as Sneddon syndrome. A child presented with global developmental delay, congenital livedo racemosa, unilateral vision loss, and a past history of focal neurological deficit. Our main objective is to make physicians aware of this nature of presentation in children and how to differentiate it from similar neurocutaneous disorders.

Biography

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