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Partial Encephalocraniocutaneous Lipomatosis Syndrome
Encephalocranial lipomatosis is a rare disorder that characteristically involves ectomesodermal tissues such as skin, eye, and the central nervous system. Here, we report a 3-year-old girl presented with developmental delay, seizures, limbal dermoid, and weakness of right lower limb. Imaging reveale...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5437771/ https://www.ncbi.nlm.nih.gov/pubmed/28553398 http://dx.doi.org/10.4103/jpn.JPN_130_16 |
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author | Velusamy, S. Bharathi, S. Sindhu Krishnakumar, B. |
author_facet | Velusamy, S. Bharathi, S. Sindhu Krishnakumar, B. |
author_sort | Velusamy, S. |
collection | PubMed |
description | Encephalocranial lipomatosis is a rare disorder that characteristically involves ectomesodermal tissues such as skin, eye, and the central nervous system. Here, we report a 3-year-old girl presented with developmental delay, seizures, limbal dermoid, and weakness of right lower limb. Imaging revealed hemiatrophy, arachnoid cyst, and polymicrogyria. The constellation of clinical finding and imaging leads to the diagnosis. |
format | Online Article Text |
id | pubmed-5437771 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-54377712017-05-26 Partial Encephalocraniocutaneous Lipomatosis Syndrome Velusamy, S. Bharathi, S. Sindhu Krishnakumar, B. J Pediatr Neurosci Case Report Encephalocranial lipomatosis is a rare disorder that characteristically involves ectomesodermal tissues such as skin, eye, and the central nervous system. Here, we report a 3-year-old girl presented with developmental delay, seizures, limbal dermoid, and weakness of right lower limb. Imaging revealed hemiatrophy, arachnoid cyst, and polymicrogyria. The constellation of clinical finding and imaging leads to the diagnosis. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5437771/ /pubmed/28553398 http://dx.doi.org/10.4103/jpn.JPN_130_16 Text en Copyright: © 2017 Journal of Pediatric Neurosciences 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-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Velusamy, S. Bharathi, S. Sindhu Krishnakumar, B. Partial Encephalocraniocutaneous Lipomatosis Syndrome |
title | Partial Encephalocraniocutaneous Lipomatosis Syndrome |
title_full | Partial Encephalocraniocutaneous Lipomatosis Syndrome |
title_fullStr | Partial Encephalocraniocutaneous Lipomatosis Syndrome |
title_full_unstemmed | Partial Encephalocraniocutaneous Lipomatosis Syndrome |
title_short | Partial Encephalocraniocutaneous Lipomatosis Syndrome |
title_sort | partial encephalocraniocutaneous lipomatosis syndrome |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5437771/ https://www.ncbi.nlm.nih.gov/pubmed/28553398 http://dx.doi.org/10.4103/jpn.JPN_130_16 |
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