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Early Manifestation of Supravalvular Aortic and Pulmonary Artery Stenosis in a Patient with Williams Syndrome

Williams syndrome (WS) is a developmental disorder characterized by vascular abnormalities such as thickening of the vascular media layer in medium- and large-sized arteries. Supravalvular aortic stenosis (SVAS) and peripheral pulmonary artery stenosis (PPAS) are common vascular abnormalities in WS....

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Autores principales: Lee, Jong Uk, Jang, Woo Sung, Lee, Young Ok, Cho, Joon Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Thoracic and Cardiovascular Surgery 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4825913/
https://www.ncbi.nlm.nih.gov/pubmed/27066434
http://dx.doi.org/10.5090/kjtcs.2016.49.1.115
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author Lee, Jong Uk
Jang, Woo Sung
Lee, Young Ok
Cho, Joon Yong
author_facet Lee, Jong Uk
Jang, Woo Sung
Lee, Young Ok
Cho, Joon Yong
author_sort Lee, Jong Uk
collection PubMed
description Williams syndrome (WS) is a developmental disorder characterized by vascular abnormalities such as thickening of the vascular media layer in medium- and large-sized arteries. Supravalvular aortic stenosis (SVAS) and peripheral pulmonary artery stenosis (PPAS) are common vascular abnormalities in WS. The natural course of SVAS and PPAS is variable, and the timing of surgery or intervention is determined according to the progression of vascular stenosis. In our patient, SVAS and PPAS showed rapid concurrent progression within two weeks after birth. We report the early manifestation of SVAS and PPAS in the neonatal period and describe the surgical treatment for stenosis relief.
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spelling pubmed-48259132016-04-08 Early Manifestation of Supravalvular Aortic and Pulmonary Artery Stenosis in a Patient with Williams Syndrome Lee, Jong Uk Jang, Woo Sung Lee, Young Ok Cho, Joon Yong Korean J Thorac Cardiovasc Surg Case Report Williams syndrome (WS) is a developmental disorder characterized by vascular abnormalities such as thickening of the vascular media layer in medium- and large-sized arteries. Supravalvular aortic stenosis (SVAS) and peripheral pulmonary artery stenosis (PPAS) are common vascular abnormalities in WS. The natural course of SVAS and PPAS is variable, and the timing of surgery or intervention is determined according to the progression of vascular stenosis. In our patient, SVAS and PPAS showed rapid concurrent progression within two weeks after birth. We report the early manifestation of SVAS and PPAS in the neonatal period and describe the surgical treatment for stenosis relief. The Korean Society for Thoracic and Cardiovascular Surgery 2016-04 2016-02-05 /pmc/articles/PMC4825913/ /pubmed/27066434 http://dx.doi.org/10.5090/kjtcs.2016.49.1.115 Text en Copyright © 2016 by The Korean Society for Thoracic and Cardiovascular Surgery. All rights Reserved. This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creative-commons.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 Case Report
Lee, Jong Uk
Jang, Woo Sung
Lee, Young Ok
Cho, Joon Yong
Early Manifestation of Supravalvular Aortic and Pulmonary Artery Stenosis in a Patient with Williams Syndrome
title Early Manifestation of Supravalvular Aortic and Pulmonary Artery Stenosis in a Patient with Williams Syndrome
title_full Early Manifestation of Supravalvular Aortic and Pulmonary Artery Stenosis in a Patient with Williams Syndrome
title_fullStr Early Manifestation of Supravalvular Aortic and Pulmonary Artery Stenosis in a Patient with Williams Syndrome
title_full_unstemmed Early Manifestation of Supravalvular Aortic and Pulmonary Artery Stenosis in a Patient with Williams Syndrome
title_short Early Manifestation of Supravalvular Aortic and Pulmonary Artery Stenosis in a Patient with Williams Syndrome
title_sort early manifestation of supravalvular aortic and pulmonary artery stenosis in a patient with williams syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4825913/
https://www.ncbi.nlm.nih.gov/pubmed/27066434
http://dx.doi.org/10.5090/kjtcs.2016.49.1.115
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