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An online compendium of treatable genetic disorders
More than 4,000 genes have been associated with recognizable Mendelian/monogenic diseases. When faced with a new diagnosis of a rare genetic disorder, health care providers increasingly turn to internet resources for information to understand the disease and direct care. Unfortunately, it can be cha...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7986124/ https://www.ncbi.nlm.nih.gov/pubmed/33350578 http://dx.doi.org/10.1002/ajmg.c.31874 |
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author | Bick, David Bick, Sarah L. Dimmock, David P. Fowler, Tom A. Caulfield, Mark J. Scott, Richard H. |
author_facet | Bick, David Bick, Sarah L. Dimmock, David P. Fowler, Tom A. Caulfield, Mark J. Scott, Richard H. |
author_sort | Bick, David |
collection | PubMed |
description | More than 4,000 genes have been associated with recognizable Mendelian/monogenic diseases. When faced with a new diagnosis of a rare genetic disorder, health care providers increasingly turn to internet resources for information to understand the disease and direct care. Unfortunately, it can be challenging to find information concerning treatment for rare diseases as key details are scattered across a number of authoritative websites and numerous journal articles. The website and associated mobile device application described in this article begin to address this challenge by providing a convenient, readily available starting point to find treatment information. The site, Rx-genes.com (https://www.rx-genes.com/), is focused on those conditions where the treatment is directed against the mechanism of the disease and thereby alters the natural history of the disease. The website currently contains 633 disease entries that include references to disease information and treatment guidance, a brief summary of treatments, the inheritance pattern, a disease frequency (if known), nonmolecular confirmatory testing (if available), and a link to experimental treatments. Existing entries are continuously updated, and new entries are added as novel treatments appear in the literature. |
format | Online Article Text |
id | pubmed-7986124 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79861242021-03-25 An online compendium of treatable genetic disorders Bick, David Bick, Sarah L. Dimmock, David P. Fowler, Tom A. Caulfield, Mark J. Scott, Richard H. Am J Med Genet C Semin Med Genet Research Articles More than 4,000 genes have been associated with recognizable Mendelian/monogenic diseases. When faced with a new diagnosis of a rare genetic disorder, health care providers increasingly turn to internet resources for information to understand the disease and direct care. Unfortunately, it can be challenging to find information concerning treatment for rare diseases as key details are scattered across a number of authoritative websites and numerous journal articles. The website and associated mobile device application described in this article begin to address this challenge by providing a convenient, readily available starting point to find treatment information. The site, Rx-genes.com (https://www.rx-genes.com/), is focused on those conditions where the treatment is directed against the mechanism of the disease and thereby alters the natural history of the disease. The website currently contains 633 disease entries that include references to disease information and treatment guidance, a brief summary of treatments, the inheritance pattern, a disease frequency (if known), nonmolecular confirmatory testing (if available), and a link to experimental treatments. Existing entries are continuously updated, and new entries are added as novel treatments appear in the literature. John Wiley & Sons, Inc. 2020-12-22 2021-03 /pmc/articles/PMC7986124/ /pubmed/33350578 http://dx.doi.org/10.1002/ajmg.c.31874 Text en © 2021 The Authors. American Journal of Medical Genetics Part C: Seminars in Medical Genetics published by Wiley Periodicals LLC. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Bick, David Bick, Sarah L. Dimmock, David P. Fowler, Tom A. Caulfield, Mark J. Scott, Richard H. An online compendium of treatable genetic disorders |
title | An online compendium of treatable genetic disorders |
title_full | An online compendium of treatable genetic disorders |
title_fullStr | An online compendium of treatable genetic disorders |
title_full_unstemmed | An online compendium of treatable genetic disorders |
title_short | An online compendium of treatable genetic disorders |
title_sort | online compendium of treatable genetic disorders |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7986124/ https://www.ncbi.nlm.nih.gov/pubmed/33350578 http://dx.doi.org/10.1002/ajmg.c.31874 |
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