Maheshwari Nallur SiddarajuKaiser Permanente, USA
Title: An eight-year-old child with Sneddon syndrome: A rare case report
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.
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