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Reading and Language Disorders: The Importance of Both Quantity and Quality
Reading and language disorders are common childhood conditions that often co-occur with each other and with other neurodevelopmental impairments. There is strong evidence that disorders, such as dyslexia and Specific Language Impairment (SLI), have a genetic basis, but we expect the contributing gen...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4094934/ https://www.ncbi.nlm.nih.gov/pubmed/24705331 http://dx.doi.org/10.3390/genes5020285 |
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author | Newbury, Dianne F. Monaco, Anthony P. Paracchini, Silvia |
author_facet | Newbury, Dianne F. Monaco, Anthony P. Paracchini, Silvia |
author_sort | Newbury, Dianne F. |
collection | PubMed |
description | Reading and language disorders are common childhood conditions that often co-occur with each other and with other neurodevelopmental impairments. There is strong evidence that disorders, such as dyslexia and Specific Language Impairment (SLI), have a genetic basis, but we expect the contributing genetic factors to be complex in nature. To date, only a few genes have been implicated in these traits. Their functional characterization has provided novel insight into the biology of neurodevelopmental disorders. However, the lack of biological markers and clear diagnostic criteria have prevented the collection of the large sample sizes required for well-powered genome-wide screens. One of the main challenges of the field will be to combine careful clinical assessment with high throughput genetic technologies within multidisciplinary collaborations. |
format | Online Article Text |
id | pubmed-4094934 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-40949342014-07-14 Reading and Language Disorders: The Importance of Both Quantity and Quality Newbury, Dianne F. Monaco, Anthony P. Paracchini, Silvia Genes (Basel) Review Reading and language disorders are common childhood conditions that often co-occur with each other and with other neurodevelopmental impairments. There is strong evidence that disorders, such as dyslexia and Specific Language Impairment (SLI), have a genetic basis, but we expect the contributing genetic factors to be complex in nature. To date, only a few genes have been implicated in these traits. Their functional characterization has provided novel insight into the biology of neurodevelopmental disorders. However, the lack of biological markers and clear diagnostic criteria have prevented the collection of the large sample sizes required for well-powered genome-wide screens. One of the main challenges of the field will be to combine careful clinical assessment with high throughput genetic technologies within multidisciplinary collaborations. MDPI 2014-04-04 /pmc/articles/PMC4094934/ /pubmed/24705331 http://dx.doi.org/10.3390/genes5020285 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review Newbury, Dianne F. Monaco, Anthony P. Paracchini, Silvia Reading and Language Disorders: The Importance of Both Quantity and Quality |
title | Reading and Language Disorders: The Importance of Both Quantity and Quality |
title_full | Reading and Language Disorders: The Importance of Both Quantity and Quality |
title_fullStr | Reading and Language Disorders: The Importance of Both Quantity and Quality |
title_full_unstemmed | Reading and Language Disorders: The Importance of Both Quantity and Quality |
title_short | Reading and Language Disorders: The Importance of Both Quantity and Quality |
title_sort | reading and language disorders: the importance of both quantity and quality |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4094934/ https://www.ncbi.nlm.nih.gov/pubmed/24705331 http://dx.doi.org/10.3390/genes5020285 |
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