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Genetic regulation of linear growth

Linear growth occurs at the growth plate. Therefore, genetic defects that interfere with the normal function of the growth plate can cause linear growth disorders. Many genetic causes of growth disorders have already been identified in humans. However, recent genome-wide approaches have broadened ou...

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Detalles Bibliográficos
Autores principales: Yue, Shanna, Whalen, Philip, Jee, Youn Hee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Pediatric Endocrinology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6449614/
https://www.ncbi.nlm.nih.gov/pubmed/30943674
http://dx.doi.org/10.6065/apem.2019.24.1.2
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author Yue, Shanna
Whalen, Philip
Jee, Youn Hee
author_facet Yue, Shanna
Whalen, Philip
Jee, Youn Hee
author_sort Yue, Shanna
collection PubMed
description Linear growth occurs at the growth plate. Therefore, genetic defects that interfere with the normal function of the growth plate can cause linear growth disorders. Many genetic causes of growth disorders have already been identified in humans. However, recent genome-wide approaches have broadened our knowledge of the mechanisms of linear growth, not only providing novel monogenic causes of growth disorders but also revealing single nucleotide polymorphisms in genes that affect height in the general population. The genes identified as causative of linear growth disorders are heterogeneous, playing a role in various growth-regulating mechanisms including those involving the extracellular matrix, intracellular signaling, paracrine signaling, endocrine signaling, and epigenetic regulation. Understanding the underlying genetic defects in linear growth is important for clinicians and researchers in order to provide proper diagnoses, management, and genetic counseling, as well as to develop better treatment approaches for children with growth disorders.
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spelling pubmed-64496142019-04-10 Genetic regulation of linear growth Yue, Shanna Whalen, Philip Jee, Youn Hee Ann Pediatr Endocrinol Metab Review Article Linear growth occurs at the growth plate. Therefore, genetic defects that interfere with the normal function of the growth plate can cause linear growth disorders. Many genetic causes of growth disorders have already been identified in humans. However, recent genome-wide approaches have broadened our knowledge of the mechanisms of linear growth, not only providing novel monogenic causes of growth disorders but also revealing single nucleotide polymorphisms in genes that affect height in the general population. The genes identified as causative of linear growth disorders are heterogeneous, playing a role in various growth-regulating mechanisms including those involving the extracellular matrix, intracellular signaling, paracrine signaling, endocrine signaling, and epigenetic regulation. Understanding the underlying genetic defects in linear growth is important for clinicians and researchers in order to provide proper diagnoses, management, and genetic counseling, as well as to develop better treatment approaches for children with growth disorders. Korean Society of Pediatric Endocrinology 2019-03 2019-03-31 /pmc/articles/PMC6449614/ /pubmed/30943674 http://dx.doi.org/10.6065/apem.2019.24.1.2 Text en © 2019 Annals of Pediatric Endocrinology & Metabolism This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Yue, Shanna
Whalen, Philip
Jee, Youn Hee
Genetic regulation of linear growth
title Genetic regulation of linear growth
title_full Genetic regulation of linear growth
title_fullStr Genetic regulation of linear growth
title_full_unstemmed Genetic regulation of linear growth
title_short Genetic regulation of linear growth
title_sort genetic regulation of linear growth
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6449614/
https://www.ncbi.nlm.nih.gov/pubmed/30943674
http://dx.doi.org/10.6065/apem.2019.24.1.2
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