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Generalized arterial calcification of infancy and pseudoxanthoma elasticum: two sides of the same coin
Generalized arterial calcification of infancy (GACI) is associated with biallelic mutations in ENPP1 in the majority of cases, whereas mutations in ABCC6 (ATP-binding cassette subfamily C number 6) are known to cause pseudoxanthoma elasticum (PXE). However, ABCC6 mutations account for a significant...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3529400/ https://www.ncbi.nlm.nih.gov/pubmed/23269929 http://dx.doi.org/10.3389/fgene.2012.00302 |
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author | Nitschke, Yvonne Rutsch, Frank |
author_facet | Nitschke, Yvonne Rutsch, Frank |
author_sort | Nitschke, Yvonne |
collection | PubMed |
description | Generalized arterial calcification of infancy (GACI) is associated with biallelic mutations in ENPP1 in the majority of cases, whereas mutations in ABCC6 (ATP-binding cassette subfamily C number 6) are known to cause pseudoxanthoma elasticum (PXE). However, ABCC6 mutations account for a significant subset of GACI cases, and ENPP1 mutations can also be associated with PXE lesions. Based on the considerable overlap of GACI and PXE, both entities appear to reflect two ends of a clinical spectrum of ectopic calcification rather than two distinct disorders. ABCC6 and ENPP1 mutations might lead to alterations of the same physiological pathways. |
format | Online Article Text |
id | pubmed-3529400 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-35294002012-12-26 Generalized arterial calcification of infancy and pseudoxanthoma elasticum: two sides of the same coin Nitschke, Yvonne Rutsch, Frank Front Genet Physiology Generalized arterial calcification of infancy (GACI) is associated with biallelic mutations in ENPP1 in the majority of cases, whereas mutations in ABCC6 (ATP-binding cassette subfamily C number 6) are known to cause pseudoxanthoma elasticum (PXE). However, ABCC6 mutations account for a significant subset of GACI cases, and ENPP1 mutations can also be associated with PXE lesions. Based on the considerable overlap of GACI and PXE, both entities appear to reflect two ends of a clinical spectrum of ectopic calcification rather than two distinct disorders. ABCC6 and ENPP1 mutations might lead to alterations of the same physiological pathways. Frontiers Media S.A. 2012-12-24 /pmc/articles/PMC3529400/ /pubmed/23269929 http://dx.doi.org/10.3389/fgene.2012.00302 Text en Copyright © Nitschke and Rutsch. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc. |
spellingShingle | Physiology Nitschke, Yvonne Rutsch, Frank Generalized arterial calcification of infancy and pseudoxanthoma elasticum: two sides of the same coin |
title | Generalized arterial calcification of infancy and pseudoxanthoma elasticum: two sides of the same coin |
title_full | Generalized arterial calcification of infancy and pseudoxanthoma elasticum: two sides of the same coin |
title_fullStr | Generalized arterial calcification of infancy and pseudoxanthoma elasticum: two sides of the same coin |
title_full_unstemmed | Generalized arterial calcification of infancy and pseudoxanthoma elasticum: two sides of the same coin |
title_short | Generalized arterial calcification of infancy and pseudoxanthoma elasticum: two sides of the same coin |
title_sort | generalized arterial calcification of infancy and pseudoxanthoma elasticum: two sides of the same coin |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3529400/ https://www.ncbi.nlm.nih.gov/pubmed/23269929 http://dx.doi.org/10.3389/fgene.2012.00302 |
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