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MicroRNAs and intellectual disability (ID) in Down syndrome, X-linked ID, and Fragile X syndrome
Intellectual disability (ID) is one of the many features manifested in various genetic syndromes leading to deficits in cognitive function among affected individuals. ID is a feature affected by polygenes and multiple environmental factors. It leads to a broad spectrum of affected clinical and behav...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3625835/ https://www.ncbi.nlm.nih.gov/pubmed/23596395 http://dx.doi.org/10.3389/fncel.2013.00041 |
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author | Siew, Wei-Hong Tan, Kai-Leng Babaei, Maryam Abbaspour Cheah, Pike-See Ling, King-Hwa |
author_facet | Siew, Wei-Hong Tan, Kai-Leng Babaei, Maryam Abbaspour Cheah, Pike-See Ling, King-Hwa |
author_sort | Siew, Wei-Hong |
collection | PubMed |
description | Intellectual disability (ID) is one of the many features manifested in various genetic syndromes leading to deficits in cognitive function among affected individuals. ID is a feature affected by polygenes and multiple environmental factors. It leads to a broad spectrum of affected clinical and behavioral characteristics among patients. Until now, the causative mechanism of ID is unknown and the progression of the condition is poorly understood. Advancement in technology and research had identified various genetic abnormalities and defects as the potential cause of ID. However, the link between these abnormalities with ID is remained inconclusive and the roles of many newly discovered genetic components such as non-coding RNAs have not been thoroughly investigated. In this review, we aim to consolidate and assimilate the latest development and findings on a class of small non-coding RNAs known as microRNAs (miRNAs) involvement in ID development and progression with special focus on Down syndrome (DS) and X-linked ID (XLID) [including Fragile X syndrome (FXS)]. |
format | Online Article Text |
id | pubmed-3625835 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-36258352013-04-17 MicroRNAs and intellectual disability (ID) in Down syndrome, X-linked ID, and Fragile X syndrome Siew, Wei-Hong Tan, Kai-Leng Babaei, Maryam Abbaspour Cheah, Pike-See Ling, King-Hwa Front Cell Neurosci Neuroscience Intellectual disability (ID) is one of the many features manifested in various genetic syndromes leading to deficits in cognitive function among affected individuals. ID is a feature affected by polygenes and multiple environmental factors. It leads to a broad spectrum of affected clinical and behavioral characteristics among patients. Until now, the causative mechanism of ID is unknown and the progression of the condition is poorly understood. Advancement in technology and research had identified various genetic abnormalities and defects as the potential cause of ID. However, the link between these abnormalities with ID is remained inconclusive and the roles of many newly discovered genetic components such as non-coding RNAs have not been thoroughly investigated. In this review, we aim to consolidate and assimilate the latest development and findings on a class of small non-coding RNAs known as microRNAs (miRNAs) involvement in ID development and progression with special focus on Down syndrome (DS) and X-linked ID (XLID) [including Fragile X syndrome (FXS)]. Frontiers Media S.A. 2013-04-15 /pmc/articles/PMC3625835/ /pubmed/23596395 http://dx.doi.org/10.3389/fncel.2013.00041 Text en Copyright © 2013 Siew, Tan, Abbaspour Babaei, Cheah and Ling. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc. |
spellingShingle | Neuroscience Siew, Wei-Hong Tan, Kai-Leng Babaei, Maryam Abbaspour Cheah, Pike-See Ling, King-Hwa MicroRNAs and intellectual disability (ID) in Down syndrome, X-linked ID, and Fragile X syndrome |
title | MicroRNAs and intellectual disability (ID) in Down syndrome, X-linked ID, and Fragile X syndrome |
title_full | MicroRNAs and intellectual disability (ID) in Down syndrome, X-linked ID, and Fragile X syndrome |
title_fullStr | MicroRNAs and intellectual disability (ID) in Down syndrome, X-linked ID, and Fragile X syndrome |
title_full_unstemmed | MicroRNAs and intellectual disability (ID) in Down syndrome, X-linked ID, and Fragile X syndrome |
title_short | MicroRNAs and intellectual disability (ID) in Down syndrome, X-linked ID, and Fragile X syndrome |
title_sort | micrornas and intellectual disability (id) in down syndrome, x-linked id, and fragile x syndrome |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3625835/ https://www.ncbi.nlm.nih.gov/pubmed/23596395 http://dx.doi.org/10.3389/fncel.2013.00041 |
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