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Speckled lentiginous nevus syndrome with median nerve paresis: A rare syndrome with a new association
Speckled lentiginous nevus (SLN) represents a mosaic phenotype which consists of café au lait macule superimposed by melanocytic nevi. Recently, SLN syndrome has been characterized where ipsilateral neurological abnormalities have been reported in association with SLN with papular type of melanocyti...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3752487/ https://www.ncbi.nlm.nih.gov/pubmed/23984245 http://dx.doi.org/10.4103/2229-5178.115530 |
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author | Mendiratta, Vibhu Jabeen, Masarat Barara, Meenu Varshney, Manish |
author_facet | Mendiratta, Vibhu Jabeen, Masarat Barara, Meenu Varshney, Manish |
author_sort | Mendiratta, Vibhu |
collection | PubMed |
description | Speckled lentiginous nevus (SLN) represents a mosaic phenotype which consists of café au lait macule superimposed by melanocytic nevi. Recently, SLN syndrome has been characterized where ipsilateral neurological abnormalities have been reported in association with SLN with papular type of melanocytic nevi only. This case describes the presence of ipsilateral thenar muscle atrophy with median nerve paresis in nevus spilus which had melanocytic nevi of the macular type alone, thus delineating a new association in SLN syndrome, hitherto unreported. |
format | Online Article Text |
id | pubmed-3752487 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-37524872013-08-27 Speckled lentiginous nevus syndrome with median nerve paresis: A rare syndrome with a new association Mendiratta, Vibhu Jabeen, Masarat Barara, Meenu Varshney, Manish Indian Dermatol Online J Case Report Speckled lentiginous nevus (SLN) represents a mosaic phenotype which consists of café au lait macule superimposed by melanocytic nevi. Recently, SLN syndrome has been characterized where ipsilateral neurological abnormalities have been reported in association with SLN with papular type of melanocytic nevi only. This case describes the presence of ipsilateral thenar muscle atrophy with median nerve paresis in nevus spilus which had melanocytic nevi of the macular type alone, thus delineating a new association in SLN syndrome, hitherto unreported. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3752487/ /pubmed/23984245 http://dx.doi.org/10.4103/2229-5178.115530 Text en Copyright: © Indian Dermatology Online Journal http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Mendiratta, Vibhu Jabeen, Masarat Barara, Meenu Varshney, Manish Speckled lentiginous nevus syndrome with median nerve paresis: A rare syndrome with a new association |
title | Speckled lentiginous nevus syndrome with median nerve paresis: A rare syndrome with a new association |
title_full | Speckled lentiginous nevus syndrome with median nerve paresis: A rare syndrome with a new association |
title_fullStr | Speckled lentiginous nevus syndrome with median nerve paresis: A rare syndrome with a new association |
title_full_unstemmed | Speckled lentiginous nevus syndrome with median nerve paresis: A rare syndrome with a new association |
title_short | Speckled lentiginous nevus syndrome with median nerve paresis: A rare syndrome with a new association |
title_sort | speckled lentiginous nevus syndrome with median nerve paresis: a rare syndrome with a new association |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3752487/ https://www.ncbi.nlm.nih.gov/pubmed/23984245 http://dx.doi.org/10.4103/2229-5178.115530 |
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