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Complete Corpus Callosum Agenesis: Can It Be Mild?
Corpus callosum agenesis is a relatively common brain malformation. It can be isolated or included in a complex alteration of brain (or sometimes even whole body) morphology. Etiology and pathogenetic mechanisms have been better understood in recent years due to the availability of more adequate ani...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3437615/ https://www.ncbi.nlm.nih.gov/pubmed/22973527 http://dx.doi.org/10.1155/2012/752751 |
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author | Chiappedi, Matteo Fresca, Anna Baschenis, Ilaria Maria Carlotta |
author_facet | Chiappedi, Matteo Fresca, Anna Baschenis, Ilaria Maria Carlotta |
author_sort | Chiappedi, Matteo |
collection | PubMed |
description | Corpus callosum agenesis is a relatively common brain malformation. It can be isolated or included in a complex alteration of brain (or sometimes even whole body) morphology. Etiology and pathogenetic mechanisms have been better understood in recent years due to the availability of more adequate animal models and the relevant progresses in developmental neurosciences. We present the case of a girl with a complete agenesis of the corpus callosum discovered at birth. She had mild learning difficulties, but reached satisfactory levels of autonomy after an individually tailored rehabilitative treatment. Her story is discussed in light of recent findings, which emphasize the possibility to exploit brain plasticity and the utility of an individually tailored approach, defined on the basis of a dialogue with the family and the patient. |
format | Online Article Text |
id | pubmed-3437615 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-34376152012-09-12 Complete Corpus Callosum Agenesis: Can It Be Mild? Chiappedi, Matteo Fresca, Anna Baschenis, Ilaria Maria Carlotta Case Rep Pediatr Case Report Corpus callosum agenesis is a relatively common brain malformation. It can be isolated or included in a complex alteration of brain (or sometimes even whole body) morphology. Etiology and pathogenetic mechanisms have been better understood in recent years due to the availability of more adequate animal models and the relevant progresses in developmental neurosciences. We present the case of a girl with a complete agenesis of the corpus callosum discovered at birth. She had mild learning difficulties, but reached satisfactory levels of autonomy after an individually tailored rehabilitative treatment. Her story is discussed in light of recent findings, which emphasize the possibility to exploit brain plasticity and the utility of an individually tailored approach, defined on the basis of a dialogue with the family and the patient. Hindawi Publishing Corporation 2012 2012-08-29 /pmc/articles/PMC3437615/ /pubmed/22973527 http://dx.doi.org/10.1155/2012/752751 Text en Copyright © 2012 Matteo Chiappedi et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Chiappedi, Matteo Fresca, Anna Baschenis, Ilaria Maria Carlotta Complete Corpus Callosum Agenesis: Can It Be Mild? |
title | Complete Corpus Callosum Agenesis: Can It Be Mild? |
title_full | Complete Corpus Callosum Agenesis: Can It Be Mild? |
title_fullStr | Complete Corpus Callosum Agenesis: Can It Be Mild? |
title_full_unstemmed | Complete Corpus Callosum Agenesis: Can It Be Mild? |
title_short | Complete Corpus Callosum Agenesis: Can It Be Mild? |
title_sort | complete corpus callosum agenesis: can it be mild? |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3437615/ https://www.ncbi.nlm.nih.gov/pubmed/22973527 http://dx.doi.org/10.1155/2012/752751 |
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