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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...

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Detalles Bibliográficos
Autores principales: Velusamy, S., Bharathi, S. Sindhu, Krishnakumar, B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
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.
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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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