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Unilateral Cerebellar Hypoplasia: A Rare Cause of Childhood Seizures
Cerebellar malformations are a rare group of disorders with clinical heterogeneity. The usual posterior fossa malformations comprise of the cystic lesions like Dandy-walker complex, enlarged cisterna magna or arachnoid cysts. The vermis is a commonly associated structure in both cystic and non-cysti...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6935978/ https://www.ncbi.nlm.nih.gov/pubmed/31908668 http://dx.doi.org/10.4103/jpn.JPN_102_18 |
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author | Shaikh, Minhaj Khera, Pushpinder Panda, Samhita |
author_facet | Shaikh, Minhaj Khera, Pushpinder Panda, Samhita |
author_sort | Shaikh, Minhaj |
collection | PubMed |
description | Cerebellar malformations are a rare group of disorders with clinical heterogeneity. The usual posterior fossa malformations comprise of the cystic lesions like Dandy-walker complex, enlarged cisterna magna or arachnoid cysts. The vermis is a commonly associated structure in both cystic and non-cystic posterior fossa malformations. The congenital malformations affecting the cerebellar parenchyma are however very rare. Magnetic resonance imaging (MRI) is an excellent modality to detect and accurately classify these malformations. We describe a case of 14 years old boy with unilateral cerebellar hypoplasia and recurrent seizures with emphasis on the MRI features of this rare entity. |
format | Online Article Text |
id | pubmed-6935978 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-69359782020-01-06 Unilateral Cerebellar Hypoplasia: A Rare Cause of Childhood Seizures Shaikh, Minhaj Khera, Pushpinder Panda, Samhita J Pediatr Neurosci Case Report Cerebellar malformations are a rare group of disorders with clinical heterogeneity. The usual posterior fossa malformations comprise of the cystic lesions like Dandy-walker complex, enlarged cisterna magna or arachnoid cysts. The vermis is a commonly associated structure in both cystic and non-cystic posterior fossa malformations. The congenital malformations affecting the cerebellar parenchyma are however very rare. Magnetic resonance imaging (MRI) is an excellent modality to detect and accurately classify these malformations. We describe a case of 14 years old boy with unilateral cerebellar hypoplasia and recurrent seizures with emphasis on the MRI features of this rare entity. Wolters Kluwer - Medknow 2019 2019-12-03 /pmc/articles/PMC6935978/ /pubmed/31908668 http://dx.doi.org/10.4103/jpn.JPN_102_18 Text en Copyright: © 2019 Journal of Pediatric Neurosciences http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Shaikh, Minhaj Khera, Pushpinder Panda, Samhita Unilateral Cerebellar Hypoplasia: A Rare Cause of Childhood Seizures |
title | Unilateral Cerebellar Hypoplasia: A Rare Cause of Childhood Seizures |
title_full | Unilateral Cerebellar Hypoplasia: A Rare Cause of Childhood Seizures |
title_fullStr | Unilateral Cerebellar Hypoplasia: A Rare Cause of Childhood Seizures |
title_full_unstemmed | Unilateral Cerebellar Hypoplasia: A Rare Cause of Childhood Seizures |
title_short | Unilateral Cerebellar Hypoplasia: A Rare Cause of Childhood Seizures |
title_sort | unilateral cerebellar hypoplasia: a rare cause of childhood seizures |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6935978/ https://www.ncbi.nlm.nih.gov/pubmed/31908668 http://dx.doi.org/10.4103/jpn.JPN_102_18 |
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