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The pathogenesis of the clinical features of oral-facial-digital syndrome type I
Oral-facial-digital syndrome type I (OFDI) is an X-linked syndrome, which has several craniofacial and limb features; and hence, patients frequently present to craniofacial and plastic surgeons. Oral-facial-digital syndrome type I is caused by mutations in the CXORF5 gene. The gene product is one of...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Saudi Medical Journal
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4673363/ https://www.ncbi.nlm.nih.gov/pubmed/26593159 http://dx.doi.org/10.15537/smj.2015.11.12446 |
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author | AlKattan, Wael M. Al-Qattan, Mohammad M. Bafaqeeh, Sameer A. |
author_facet | AlKattan, Wael M. Al-Qattan, Mohammad M. Bafaqeeh, Sameer A. |
author_sort | AlKattan, Wael M. |
collection | PubMed |
description | Oral-facial-digital syndrome type I (OFDI) is an X-linked syndrome, which has several craniofacial and limb features; and hence, patients frequently present to craniofacial and plastic surgeons. Oral-facial-digital syndrome type I is caused by mutations in the CXORF5 gene. The gene product is one of the basal body proteins of a slim microtubule-based organelle called the “primary cilium”. Most of the clinical features of OFDI patients are related to dysfunctions of the primary cilium leading to abnormal Hedgehog signal transduction, depressed planar cell polarity pathway, and errors in cell cycle control. |
format | Online Article Text |
id | pubmed-4673363 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Saudi Medical Journal |
record_format | MEDLINE/PubMed |
spelling | pubmed-46733632015-12-10 The pathogenesis of the clinical features of oral-facial-digital syndrome type I AlKattan, Wael M. Al-Qattan, Mohammad M. Bafaqeeh, Sameer A. Saudi Med J Review Article Oral-facial-digital syndrome type I (OFDI) is an X-linked syndrome, which has several craniofacial and limb features; and hence, patients frequently present to craniofacial and plastic surgeons. Oral-facial-digital syndrome type I is caused by mutations in the CXORF5 gene. The gene product is one of the basal body proteins of a slim microtubule-based organelle called the “primary cilium”. Most of the clinical features of OFDI patients are related to dysfunctions of the primary cilium leading to abnormal Hedgehog signal transduction, depressed planar cell polarity pathway, and errors in cell cycle control. Saudi Medical Journal 2015-11 /pmc/articles/PMC4673363/ /pubmed/26593159 http://dx.doi.org/10.15537/smj.2015.11.12446 Text en Copyright: © Saudi Medical Journal http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article AlKattan, Wael M. Al-Qattan, Mohammad M. Bafaqeeh, Sameer A. The pathogenesis of the clinical features of oral-facial-digital syndrome type I |
title | The pathogenesis of the clinical features of oral-facial-digital syndrome type I |
title_full | The pathogenesis of the clinical features of oral-facial-digital syndrome type I |
title_fullStr | The pathogenesis of the clinical features of oral-facial-digital syndrome type I |
title_full_unstemmed | The pathogenesis of the clinical features of oral-facial-digital syndrome type I |
title_short | The pathogenesis of the clinical features of oral-facial-digital syndrome type I |
title_sort | pathogenesis of the clinical features of oral-facial-digital syndrome type i |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4673363/ https://www.ncbi.nlm.nih.gov/pubmed/26593159 http://dx.doi.org/10.15537/smj.2015.11.12446 |
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