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Advances in understanding – genetic basis of intellectual disability
Intellectual disability is the most common developmental disorder characterized by a congenital limitation in intellectual functioning and adaptive behavior. It often co-occurs with other mental conditions like attention deficit/hyperactivity disorder and autism spectrum disorder, and can be part of...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000Research
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4830215/ https://www.ncbi.nlm.nih.gov/pubmed/27127621 http://dx.doi.org/10.12688/f1000research.7134.1 |
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author | Chiurazzi, Pietro Pirozzi, Filomena |
author_facet | Chiurazzi, Pietro Pirozzi, Filomena |
author_sort | Chiurazzi, Pietro |
collection | PubMed |
description | Intellectual disability is the most common developmental disorder characterized by a congenital limitation in intellectual functioning and adaptive behavior. It often co-occurs with other mental conditions like attention deficit/hyperactivity disorder and autism spectrum disorder, and can be part of a malformation syndrome that affects other organs. Considering the heterogeneity of its causes (environmental and genetic), its frequency worldwide varies greatly. This review focuses on known genes underlying (syndromic and non-syndromic) intellectual disability, it provides a succinct analysis of their Gene Ontology, and it suggests the use of transcriptional profiling for the prioritization of candidate genes. |
format | Online Article Text |
id | pubmed-4830215 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | F1000Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-48302152016-04-27 Advances in understanding – genetic basis of intellectual disability Chiurazzi, Pietro Pirozzi, Filomena F1000Res Review Intellectual disability is the most common developmental disorder characterized by a congenital limitation in intellectual functioning and adaptive behavior. It often co-occurs with other mental conditions like attention deficit/hyperactivity disorder and autism spectrum disorder, and can be part of a malformation syndrome that affects other organs. Considering the heterogeneity of its causes (environmental and genetic), its frequency worldwide varies greatly. This review focuses on known genes underlying (syndromic and non-syndromic) intellectual disability, it provides a succinct analysis of their Gene Ontology, and it suggests the use of transcriptional profiling for the prioritization of candidate genes. F1000Research 2016-04-07 /pmc/articles/PMC4830215/ /pubmed/27127621 http://dx.doi.org/10.12688/f1000research.7134.1 Text en Copyright: © 2016 Chiurazzi P and Pirozzi F http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Chiurazzi, Pietro Pirozzi, Filomena Advances in understanding – genetic basis of intellectual disability |
title | Advances in understanding – genetic basis of intellectual disability |
title_full | Advances in understanding – genetic basis of intellectual disability |
title_fullStr | Advances in understanding – genetic basis of intellectual disability |
title_full_unstemmed | Advances in understanding – genetic basis of intellectual disability |
title_short | Advances in understanding – genetic basis of intellectual disability |
title_sort | advances in understanding – genetic basis of intellectual disability |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4830215/ https://www.ncbi.nlm.nih.gov/pubmed/27127621 http://dx.doi.org/10.12688/f1000research.7134.1 |
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