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Neuroimaging assessment in Down syndrome: a pictorial review

Down syndrome (DS), or trisomy 21, is the leading genetic cause of intellectual incapacity worldwide, with a reported incidence of about 1 in 1,000 to 1 in 1,100 live births. Besides the several commonly known physical features characteristic of this syndrome present at birth, DS may additionally af...

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Autores principales: Rodrigues, Marta, Nunes, Joana, Figueiredo, Sofia, Martins de Campos, António, Geraldo, Ana Filipa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6527671/
https://www.ncbi.nlm.nih.gov/pubmed/31111268
http://dx.doi.org/10.1186/s13244-019-0729-3
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author Rodrigues, Marta
Nunes, Joana
Figueiredo, Sofia
Martins de Campos, António
Geraldo, Ana Filipa
author_facet Rodrigues, Marta
Nunes, Joana
Figueiredo, Sofia
Martins de Campos, António
Geraldo, Ana Filipa
author_sort Rodrigues, Marta
collection PubMed
description Down syndrome (DS), or trisomy 21, is the leading genetic cause of intellectual incapacity worldwide, with a reported incidence of about 1 in 1,000 to 1 in 1,100 live births. Besides the several commonly known physical features characteristic of this syndrome present at birth, DS may additionally affect every organ system. In addition, despite the large number of published papers concerning this syndrome, there is scarce literature focusing specifically in the typical neuroimaging features associated with this condition. The aim of this paper is to review and systematize the distinctive characteristics and abnormalities of the central nervous system, head and neck, and spine present in DS patients that should actively be searched for and evaluated by radiologists and/or neuroradiologists.
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spelling pubmed-65276712019-05-21 Neuroimaging assessment in Down syndrome: a pictorial review Rodrigues, Marta Nunes, Joana Figueiredo, Sofia Martins de Campos, António Geraldo, Ana Filipa Insights Imaging Pictorial Review Down syndrome (DS), or trisomy 21, is the leading genetic cause of intellectual incapacity worldwide, with a reported incidence of about 1 in 1,000 to 1 in 1,100 live births. Besides the several commonly known physical features characteristic of this syndrome present at birth, DS may additionally affect every organ system. In addition, despite the large number of published papers concerning this syndrome, there is scarce literature focusing specifically in the typical neuroimaging features associated with this condition. The aim of this paper is to review and systematize the distinctive characteristics and abnormalities of the central nervous system, head and neck, and spine present in DS patients that should actively be searched for and evaluated by radiologists and/or neuroradiologists. Springer Berlin Heidelberg 2019-05-20 /pmc/articles/PMC6527671/ /pubmed/31111268 http://dx.doi.org/10.1186/s13244-019-0729-3 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Pictorial Review
Rodrigues, Marta
Nunes, Joana
Figueiredo, Sofia
Martins de Campos, António
Geraldo, Ana Filipa
Neuroimaging assessment in Down syndrome: a pictorial review
title Neuroimaging assessment in Down syndrome: a pictorial review
title_full Neuroimaging assessment in Down syndrome: a pictorial review
title_fullStr Neuroimaging assessment in Down syndrome: a pictorial review
title_full_unstemmed Neuroimaging assessment in Down syndrome: a pictorial review
title_short Neuroimaging assessment in Down syndrome: a pictorial review
title_sort neuroimaging assessment in down syndrome: a pictorial review
topic Pictorial Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6527671/
https://www.ncbi.nlm.nih.gov/pubmed/31111268
http://dx.doi.org/10.1186/s13244-019-0729-3
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