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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...

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Autores principales: Shaikh, Minhaj, Khera, Pushpinder, Panda, Samhita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2019
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.
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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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