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DNA Testing in Neurologic Diseases
DNA testing is available for a growing number of hereditary diseases in neurology and other specialties. In addition to guiding breeding decisions, DNA tests are important tools in the diagnosis of diseases, particularly in conditions for which clinical signs are relatively nonspecific. DNA testing...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4857950/ https://www.ncbi.nlm.nih.gov/pubmed/24962505 http://dx.doi.org/10.1111/jvim.12383 |
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author | O'Brien, D.P. Leeb, T. |
author_facet | O'Brien, D.P. Leeb, T. |
author_sort | O'Brien, D.P. |
collection | PubMed |
description | DNA testing is available for a growing number of hereditary diseases in neurology and other specialties. In addition to guiding breeding decisions, DNA tests are important tools in the diagnosis of diseases, particularly in conditions for which clinical signs are relatively nonspecific. DNA testing also can provide valuable insight into the risk of hereditary disease when decisions about treating comorbidities are being made. Advances in technology and bioinformatics will make broad screening for potential disease‐causing mutations available soon. As DNA tests come into more common use, it is critical that clinicians understand the proper application and interpretation of these test results. |
format | Online Article Text |
id | pubmed-4857950 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-48579502016-06-22 DNA Testing in Neurologic Diseases O'Brien, D.P. Leeb, T. J Vet Intern Med Reviews DNA testing is available for a growing number of hereditary diseases in neurology and other specialties. In addition to guiding breeding decisions, DNA tests are important tools in the diagnosis of diseases, particularly in conditions for which clinical signs are relatively nonspecific. DNA testing also can provide valuable insight into the risk of hereditary disease when decisions about treating comorbidities are being made. Advances in technology and bioinformatics will make broad screening for potential disease‐causing mutations available soon. As DNA tests come into more common use, it is critical that clinicians understand the proper application and interpretation of these test results. John Wiley and Sons Inc. 2014-06-24 2014 /pmc/articles/PMC4857950/ /pubmed/24962505 http://dx.doi.org/10.1111/jvim.12383 Text en Copyright © 2014 by the American College of Veterinary Internal Medicine |
spellingShingle | Reviews O'Brien, D.P. Leeb, T. DNA Testing in Neurologic Diseases |
title |
DNA Testing in Neurologic Diseases |
title_full |
DNA Testing in Neurologic Diseases |
title_fullStr |
DNA Testing in Neurologic Diseases |
title_full_unstemmed |
DNA Testing in Neurologic Diseases |
title_short |
DNA Testing in Neurologic Diseases |
title_sort | dna testing in neurologic diseases |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4857950/ https://www.ncbi.nlm.nih.gov/pubmed/24962505 http://dx.doi.org/10.1111/jvim.12383 |
work_keys_str_mv | AT obriendp dnatestinginneurologicdiseases AT leebt dnatestinginneurologicdiseases |