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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 awar...
Autores principales: | Nallur Siddaraju, Maheshwari, Samynathan, Archana, Kurakula, Sowjanya, Kharge, Priyadarshini, Nalla, Sanjana D |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10325693/ https://www.ncbi.nlm.nih.gov/pubmed/37425554 http://dx.doi.org/10.7759/cureus.40054 |
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