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Analogs of human genetic skin disease in domesticated animals()
Genetic skin diseases encompass a vast, complex, and ever expanding field. Recognition of the features of these diseases is important to ascertain a correct diagnosis, initiate treatment, consider genetic counseling, and refer patients to specialists when the disease may impact other areas. Because...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5555282/ https://www.ncbi.nlm.nih.gov/pubmed/28831430 http://dx.doi.org/10.1016/j.ijwd.2017.01.003 |
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author | Finch, Justin Abrams, Stephanie Finch, Amy |
author_facet | Finch, Justin Abrams, Stephanie Finch, Amy |
author_sort | Finch, Justin |
collection | PubMed |
description | Genetic skin diseases encompass a vast, complex, and ever expanding field. Recognition of the features of these diseases is important to ascertain a correct diagnosis, initiate treatment, consider genetic counseling, and refer patients to specialists when the disease may impact other areas. Because genodermatoses may present with a vast array of features, it can be bewildering to memorize them. This manuscript will explain and depict some genetic skin diseases that occur in both humans and domestic animals and offer a connection and memorization aid for physicians. In addition, we will explore how animal diseases serve as a model to uncover the mechanisms of human disease. The genetic skin diseases we will review are pigmentary mosaicism, piebaldism, albinism, Griscelli syndrome, ectodermal dysplasias, Waardenburg syndrome, and mucinosis in both humans and domesticated animals. |
format | Online Article Text |
id | pubmed-5555282 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-55552822017-08-22 Analogs of human genetic skin disease in domesticated animals() Finch, Justin Abrams, Stephanie Finch, Amy Int J Womens Dermatol Review Genetic skin diseases encompass a vast, complex, and ever expanding field. Recognition of the features of these diseases is important to ascertain a correct diagnosis, initiate treatment, consider genetic counseling, and refer patients to specialists when the disease may impact other areas. Because genodermatoses may present with a vast array of features, it can be bewildering to memorize them. This manuscript will explain and depict some genetic skin diseases that occur in both humans and domestic animals and offer a connection and memorization aid for physicians. In addition, we will explore how animal diseases serve as a model to uncover the mechanisms of human disease. The genetic skin diseases we will review are pigmentary mosaicism, piebaldism, albinism, Griscelli syndrome, ectodermal dysplasias, Waardenburg syndrome, and mucinosis in both humans and domesticated animals. Elsevier 2017-03-03 /pmc/articles/PMC5555282/ /pubmed/28831430 http://dx.doi.org/10.1016/j.ijwd.2017.01.003 Text en © 2017 Women's Dermatologic Society. Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Review Finch, Justin Abrams, Stephanie Finch, Amy Analogs of human genetic skin disease in domesticated animals() |
title | Analogs of human genetic skin disease in domesticated animals() |
title_full | Analogs of human genetic skin disease in domesticated animals() |
title_fullStr | Analogs of human genetic skin disease in domesticated animals() |
title_full_unstemmed | Analogs of human genetic skin disease in domesticated animals() |
title_short | Analogs of human genetic skin disease in domesticated animals() |
title_sort | analogs of human genetic skin disease in domesticated animals() |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5555282/ https://www.ncbi.nlm.nih.gov/pubmed/28831430 http://dx.doi.org/10.1016/j.ijwd.2017.01.003 |
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