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Joubert Syndrome Presenting With Normal Pyramidal Decussation: A Case Report

Joubert syndrome (JS) is a rare genetic disorder characterized by a congenital malformation of the hindbrain, and accompanied by axonal decussation abnormalities affecting the corticospinal tract and the superior cerebellar peduncles. To the best of our knowledge, there are no reports of normal pyra...

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Autores principales: Kim, Nam-Sik, Park, Sung-Hee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Academy of Rehabilitation Medicine 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5608679/
https://www.ncbi.nlm.nih.gov/pubmed/28971056
http://dx.doi.org/10.5535/arm.2017.41.4.701
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author Kim, Nam-Sik
Park, Sung-Hee
author_facet Kim, Nam-Sik
Park, Sung-Hee
author_sort Kim, Nam-Sik
collection PubMed
description Joubert syndrome (JS) is a rare genetic disorder characterized by a congenital malformation of the hindbrain, and accompanied by axonal decussation abnormalities affecting the corticospinal tract and the superior cerebellar peduncles. To the best of our knowledge, there are no reports of normal pyramidal decussation in JS. Here, we describe the case of an 18-year-old boy presenting midline-crossing corticospinal projections, which were considered normal corticospinal tract trajectories. Diffusion tensor imaging and motor evoked potential study analysis demonstrated the exclusive presence of decussating corticospinal projections in the patient. Based on these results, we suggest that JS might be associated with several, diverse corticospinal motor tract organization patterns.
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spelling pubmed-56086792017-10-02 Joubert Syndrome Presenting With Normal Pyramidal Decussation: A Case Report Kim, Nam-Sik Park, Sung-Hee Ann Rehabil Med Case Report Joubert syndrome (JS) is a rare genetic disorder characterized by a congenital malformation of the hindbrain, and accompanied by axonal decussation abnormalities affecting the corticospinal tract and the superior cerebellar peduncles. To the best of our knowledge, there are no reports of normal pyramidal decussation in JS. Here, we describe the case of an 18-year-old boy presenting midline-crossing corticospinal projections, which were considered normal corticospinal tract trajectories. Diffusion tensor imaging and motor evoked potential study analysis demonstrated the exclusive presence of decussating corticospinal projections in the patient. Based on these results, we suggest that JS might be associated with several, diverse corticospinal motor tract organization patterns. Korean Academy of Rehabilitation Medicine 2017-08 2017-08-31 /pmc/articles/PMC5608679/ /pubmed/28971056 http://dx.doi.org/10.5535/arm.2017.41.4.701 Text en Copyright © 2017 by Korean Academy of Rehabilitation Medicine http://creativecommons.org/licenses/by-nc/4.0 This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Kim, Nam-Sik
Park, Sung-Hee
Joubert Syndrome Presenting With Normal Pyramidal Decussation: A Case Report
title Joubert Syndrome Presenting With Normal Pyramidal Decussation: A Case Report
title_full Joubert Syndrome Presenting With Normal Pyramidal Decussation: A Case Report
title_fullStr Joubert Syndrome Presenting With Normal Pyramidal Decussation: A Case Report
title_full_unstemmed Joubert Syndrome Presenting With Normal Pyramidal Decussation: A Case Report
title_short Joubert Syndrome Presenting With Normal Pyramidal Decussation: A Case Report
title_sort joubert syndrome presenting with normal pyramidal decussation: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5608679/
https://www.ncbi.nlm.nih.gov/pubmed/28971056
http://dx.doi.org/10.5535/arm.2017.41.4.701
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