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Idiopathic arterial calcification of infancy - a case report
Idiopathic arterial calcification of infancy is a rare condition characterized by extensive calcification and stenosis of large and medium sized arteries. A ten day old female baby developed sudden shortness of breath and was treated with oxygen and antibiotics. Antenatal echocardiography showed cal...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2004
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3232550/ https://www.ncbi.nlm.nih.gov/pubmed/22368635 |
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author | Sundaram, S Kuruvilla, S Thirupuram, S |
author_facet | Sundaram, S Kuruvilla, S Thirupuram, S |
author_sort | Sundaram, S |
collection | PubMed |
description | Idiopathic arterial calcification of infancy is a rare condition characterized by extensive calcification and stenosis of large and medium sized arteries. A ten day old female baby developed sudden shortness of breath and was treated with oxygen and antibiotics. Antenatal echocardiography showed calcification of the aorta and pulmonary arteries. Autopsy examination revealed extensive calcification in the walls of major arteries and vessels of several organs. The baby was found to have a karyotype of 47 chromosomes. |
format | Online Article Text |
id | pubmed-3232550 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-32325502012-02-22 Idiopathic arterial calcification of infancy - a case report Sundaram, S Kuruvilla, S Thirupuram, S Images Paediatr Cardiol Case Report Idiopathic arterial calcification of infancy is a rare condition characterized by extensive calcification and stenosis of large and medium sized arteries. A ten day old female baby developed sudden shortness of breath and was treated with oxygen and antibiotics. Antenatal echocardiography showed calcification of the aorta and pulmonary arteries. Autopsy examination revealed extensive calcification in the walls of major arteries and vessels of several organs. The baby was found to have a karyotype of 47 chromosomes. Medknow Publications & Media Pvt Ltd 2004 /pmc/articles/PMC3232550/ /pubmed/22368635 Text en Copyright: © Images in Paediatric Cardiology 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 | Case Report Sundaram, S Kuruvilla, S Thirupuram, S Idiopathic arterial calcification of infancy - a case report |
title | Idiopathic arterial calcification of infancy - a case report |
title_full | Idiopathic arterial calcification of infancy - a case report |
title_fullStr | Idiopathic arterial calcification of infancy - a case report |
title_full_unstemmed | Idiopathic arterial calcification of infancy - a case report |
title_short | Idiopathic arterial calcification of infancy - a case report |
title_sort | idiopathic arterial calcification of infancy - a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3232550/ https://www.ncbi.nlm.nih.gov/pubmed/22368635 |
work_keys_str_mv | AT sundarams idiopathicarterialcalcificationofinfancyacasereport AT kuruvillas idiopathicarterialcalcificationofinfancyacasereport AT thirupurams idiopathicarterialcalcificationofinfancyacasereport |