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Bilateral giant open-lip schizencephaly: A rare case report
Schizencephaly is an extremely rare developmental birth defect characterized by abnormal slits or clefts in the cerebral hemispheres extending from the lateral ventricle to the cerebral cortex. The margins of the cleft are lined with heterotropic, dysplastic gray matter. The causes of schizencephaly...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4991154/ https://www.ncbi.nlm.nih.gov/pubmed/27606022 http://dx.doi.org/10.4103/1817-1745.187638 |
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author | Rege, Shrikant V. Patil, Harshad |
author_facet | Rege, Shrikant V. Patil, Harshad |
author_sort | Rege, Shrikant V. |
collection | PubMed |
description | Schizencephaly is an extremely rare developmental birth defect characterized by abnormal slits or clefts in the cerebral hemispheres extending from the lateral ventricle to the cerebral cortex. The margins of the cleft are lined with heterotropic, dysplastic gray matter. The causes of schizencephaly are heterogeneous and include teratogens, prenatal infarction/infections, maternal trauma, or EMX2 mutations. This condition is present at birth and manifests early in life. |
format | Online Article Text |
id | pubmed-4991154 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-49911542016-09-07 Bilateral giant open-lip schizencephaly: A rare case report Rege, Shrikant V. Patil, Harshad J Pediatr Neurosci Case Report Schizencephaly is an extremely rare developmental birth defect characterized by abnormal slits or clefts in the cerebral hemispheres extending from the lateral ventricle to the cerebral cortex. The margins of the cleft are lined with heterotropic, dysplastic gray matter. The causes of schizencephaly are heterogeneous and include teratogens, prenatal infarction/infections, maternal trauma, or EMX2 mutations. This condition is present at birth and manifests early in life. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC4991154/ /pubmed/27606022 http://dx.doi.org/10.4103/1817-1745.187638 Text en Copyright: © 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 Rege, Shrikant V. Patil, Harshad Bilateral giant open-lip schizencephaly: A rare case report |
title | Bilateral giant open-lip schizencephaly: A rare case report |
title_full | Bilateral giant open-lip schizencephaly: A rare case report |
title_fullStr | Bilateral giant open-lip schizencephaly: A rare case report |
title_full_unstemmed | Bilateral giant open-lip schizencephaly: A rare case report |
title_short | Bilateral giant open-lip schizencephaly: A rare case report |
title_sort | bilateral giant open-lip schizencephaly: a rare case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4991154/ https://www.ncbi.nlm.nih.gov/pubmed/27606022 http://dx.doi.org/10.4103/1817-1745.187638 |
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