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
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author Nallur Siddaraju, Maheshwari
Samynathan, Archana
Kurakula, Sowjanya
Kharge, Priyadarshini
Nalla, Sanjana D
author_facet Nallur Siddaraju, Maheshwari
Samynathan, Archana
Kurakula, Sowjanya
Kharge, Priyadarshini
Nalla, Sanjana D
author_sort Nallur Siddaraju, Maheshwari
collection PubMed
description 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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spelling pubmed-103256932023-07-07 An Eight-Year-Old Child With Sneddon Syndrome: A Rare Case Report Nallur Siddaraju, Maheshwari Samynathan, Archana Kurakula, Sowjanya Kharge, Priyadarshini Nalla, Sanjana D Cureus Dermatology 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. Cureus 2023-06-06 /pmc/articles/PMC10325693/ /pubmed/37425554 http://dx.doi.org/10.7759/cureus.40054 Text en Copyright © 2023, Nallur Siddaraju et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Dermatology
Nallur Siddaraju, Maheshwari
Samynathan, Archana
Kurakula, Sowjanya
Kharge, Priyadarshini
Nalla, Sanjana D
An Eight-Year-Old Child With Sneddon Syndrome: A Rare Case Report
title An Eight-Year-Old Child With Sneddon Syndrome: A Rare Case Report
title_full An Eight-Year-Old Child With Sneddon Syndrome: A Rare Case Report
title_fullStr An Eight-Year-Old Child With Sneddon Syndrome: A Rare Case Report
title_full_unstemmed An Eight-Year-Old Child With Sneddon Syndrome: A Rare Case Report
title_short An Eight-Year-Old Child With Sneddon Syndrome: A Rare Case Report
title_sort eight-year-old child with sneddon syndrome: a rare case report
topic Dermatology
url 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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