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Microtia epigenetics: An overview of review and new viewpoint

INTRODUCTION: Microtia is a congenital malformation of the external and middle ear caused by the abnormal development of the first and second zygomatic arch and the first sulcus. There is currently no consensus concerning the pathogenesis and etiology of microtia; genetic and environmental factors m...

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Autores principales: Chen, Xia, Zhang, Ruhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6799854/
https://www.ncbi.nlm.nih.gov/pubmed/31593107
http://dx.doi.org/10.1097/MD.0000000000017468
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author Chen, Xia
Zhang, Ruhong
author_facet Chen, Xia
Zhang, Ruhong
author_sort Chen, Xia
collection PubMed
description INTRODUCTION: Microtia is a congenital malformation of the external and middle ear caused by the abnormal development of the first and second zygomatic arch and the first sulcus. There is currently no consensus concerning the pathogenesis and etiology of microtia; genetic and environmental factors may play a role. Gene-based studies have focused on finding the genes that cause microtia and on gene function defects. However, no clear pathogenic genes have so far been identified. Microtia is multifactorial; gene function defects cannot completely explain its pathogenesis. In recent years, the epigenetic aspects of microtia have begun to receive attention. CONCLUSIONS: Analysis of the existing data suggests that certain key genes and pathways may be the underlying cause of congenital microtia. However, further exploration is needed.
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spelling pubmed-67998542019-11-18 Microtia epigenetics: An overview of review and new viewpoint Chen, Xia Zhang, Ruhong Medicine (Baltimore) 3500 INTRODUCTION: Microtia is a congenital malformation of the external and middle ear caused by the abnormal development of the first and second zygomatic arch and the first sulcus. There is currently no consensus concerning the pathogenesis and etiology of microtia; genetic and environmental factors may play a role. Gene-based studies have focused on finding the genes that cause microtia and on gene function defects. However, no clear pathogenic genes have so far been identified. Microtia is multifactorial; gene function defects cannot completely explain its pathogenesis. In recent years, the epigenetic aspects of microtia have begun to receive attention. CONCLUSIONS: Analysis of the existing data suggests that certain key genes and pathways may be the underlying cause of congenital microtia. However, further exploration is needed. Wolters Kluwer Health 2019-10-11 /pmc/articles/PMC6799854/ /pubmed/31593107 http://dx.doi.org/10.1097/MD.0000000000017468 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0
spellingShingle 3500
Chen, Xia
Zhang, Ruhong
Microtia epigenetics: An overview of review and new viewpoint
title Microtia epigenetics: An overview of review and new viewpoint
title_full Microtia epigenetics: An overview of review and new viewpoint
title_fullStr Microtia epigenetics: An overview of review and new viewpoint
title_full_unstemmed Microtia epigenetics: An overview of review and new viewpoint
title_short Microtia epigenetics: An overview of review and new viewpoint
title_sort microtia epigenetics: an overview of review and new viewpoint
topic 3500
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6799854/
https://www.ncbi.nlm.nih.gov/pubmed/31593107
http://dx.doi.org/10.1097/MD.0000000000017468
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