An Eight-Year-Old Child With Sneddon Syndrome: A Rare Case Report.
Cureus(2023)
摘要
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.
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关键词
sneddon syndrome,rare case report,rare case,child,eight-year-old
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