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Is Gorlin–Chaudhry–Moss syndrome associated with aortopathy?

Gorlin–Chaudhry–Moss syndrome (GCMS) is a rare disorder consisting of craniofacial dysostosis, hypertrichosis, underdeveloped genitalia, and ocular and dental anomalies. Recently, GCMS has been reclassified together with Fontaine syndrome as Fontaine progeroid syndrome (FPS), after a common genetic...

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Detalles Bibliográficos
Autores principales: Legué, Juno, François, Jules H M, van Rijswijk, Carla S P, van Brakel, Thomas J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7453031/
https://www.ncbi.nlm.nih.gov/pubmed/32355952
http://dx.doi.org/10.1093/ejcts/ezaa108
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author Legué, Juno
François, Jules H M
van Rijswijk, Carla S P
van Brakel, Thomas J
author_facet Legué, Juno
François, Jules H M
van Rijswijk, Carla S P
van Brakel, Thomas J
author_sort Legué, Juno
collection PubMed
description Gorlin–Chaudhry–Moss syndrome (GCMS) is a rare disorder consisting of craniofacial dysostosis, hypertrichosis, underdeveloped genitalia, and ocular and dental anomalies. Recently, GCMS has been reclassified together with Fontaine syndrome as Fontaine progeroid syndrome (FPS), after a common genetic basis was found. It was previously thought that GCMS/FPS was not associated with aortopathy, but in recent years 3 patients with aortic disease have been described. We describe the fourth case, who is the oldest patient with GCMS/FPS reported in the medical literature: a 45-year-old patient who presented with acute aortic dissection. We therefore recommend screening patients previously diagnosed with GCMS/FPS for aortic pathology to aid early detection and avoid patient presentation in an acute setting.
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spelling pubmed-74530312020-09-01 Is Gorlin–Chaudhry–Moss syndrome associated with aortopathy? Legué, Juno François, Jules H M van Rijswijk, Carla S P van Brakel, Thomas J Eur J Cardiothorac Surg Case Reports Gorlin–Chaudhry–Moss syndrome (GCMS) is a rare disorder consisting of craniofacial dysostosis, hypertrichosis, underdeveloped genitalia, and ocular and dental anomalies. Recently, GCMS has been reclassified together with Fontaine syndrome as Fontaine progeroid syndrome (FPS), after a common genetic basis was found. It was previously thought that GCMS/FPS was not associated with aortopathy, but in recent years 3 patients with aortic disease have been described. We describe the fourth case, who is the oldest patient with GCMS/FPS reported in the medical literature: a 45-year-old patient who presented with acute aortic dissection. We therefore recommend screening patients previously diagnosed with GCMS/FPS for aortic pathology to aid early detection and avoid patient presentation in an acute setting. Oxford University Press 2020-05-01 /pmc/articles/PMC7453031/ /pubmed/32355952 http://dx.doi.org/10.1093/ejcts/ezaa108 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the European Association for Cardio-Thoracic Surgery. 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 (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Case Reports
Legué, Juno
François, Jules H M
van Rijswijk, Carla S P
van Brakel, Thomas J
Is Gorlin–Chaudhry–Moss syndrome associated with aortopathy?
title Is Gorlin–Chaudhry–Moss syndrome associated with aortopathy?
title_full Is Gorlin–Chaudhry–Moss syndrome associated with aortopathy?
title_fullStr Is Gorlin–Chaudhry–Moss syndrome associated with aortopathy?
title_full_unstemmed Is Gorlin–Chaudhry–Moss syndrome associated with aortopathy?
title_short Is Gorlin–Chaudhry–Moss syndrome associated with aortopathy?
title_sort is gorlin–chaudhry–moss syndrome associated with aortopathy?
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7453031/
https://www.ncbi.nlm.nih.gov/pubmed/32355952
http://dx.doi.org/10.1093/ejcts/ezaa108
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