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...

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Detalles Bibliográficos
Autores principales: Nallur Siddaraju, Maheshwari, Samynathan, Archana, Kurakula, Sowjanya, Kharge, Priyadarshini, Nalla, Sanjana D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Dermatology
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

Internet

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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