Marfan Syndrome: A Case Report
Marfan syndrome is an autosomal dominant systemic disorder of the connective tissue. Children affected by the Marfan syndrome carry a mutation in one of their two copies of the gene that encodes the connective tissue protein fibrillin-1. Marfan syndrome affects most organs and tissues, especially th...
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Series: | Case Reports in Dentistry |
Online Access: | http://dx.doi.org/10.1155/2012/595343 |
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doaj-9f9d4051e23d4f0d9dbe6fd6bd61bfc72021-07-02T04:20:16ZengHindawi LimitedCase Reports in Dentistry2090-64472090-64552012-01-01201210.1155/2012/595343595343Marfan Syndrome: A Case ReportRajendran Ganesh0Rajendran Vijayakumar1Haridoss Selvakumar2Department of Pedodontics, SRM Dental College, SRM University, Chennai 600078, IndiaDepartment of Pedodontics, SRM Dental College, SRM University, Chennai 600078, IndiaDepartment of Pedodontics, SRM Dental College, SRM University, Chennai 600078, IndiaMarfan syndrome is an autosomal dominant systemic disorder of the connective tissue. Children affected by the Marfan syndrome carry a mutation in one of their two copies of the gene that encodes the connective tissue protein fibrillin-1. Marfan syndrome affects most organs and tissues, especially the skeleton, lungs, eyes, heart, and the large blood vessel that distributes blood from the heart to the rest of the body. A case report of Marfan syndrome has been reported with oral features. The dental problems of the child were treated under general anesthesia and a one-month review showed intact stainless steel crowns' restorations and no signs of secondary caries.http://dx.doi.org/10.1155/2012/595343 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Rajendran Ganesh Rajendran Vijayakumar Haridoss Selvakumar |
spellingShingle |
Rajendran Ganesh Rajendran Vijayakumar Haridoss Selvakumar Marfan Syndrome: A Case Report Case Reports in Dentistry |
author_facet |
Rajendran Ganesh Rajendran Vijayakumar Haridoss Selvakumar |
author_sort |
Rajendran Ganesh |
title |
Marfan Syndrome: A Case Report |
title_short |
Marfan Syndrome: A Case Report |
title_full |
Marfan Syndrome: A Case Report |
title_fullStr |
Marfan Syndrome: A Case Report |
title_full_unstemmed |
Marfan Syndrome: A Case Report |
title_sort |
marfan syndrome: a case report |
publisher |
Hindawi Limited |
series |
Case Reports in Dentistry |
issn |
2090-6447 2090-6455 |
publishDate |
2012-01-01 |
description |
Marfan syndrome is an autosomal dominant systemic disorder of the connective tissue. Children affected by the Marfan syndrome carry a mutation in one of their two copies of the gene that encodes the connective tissue protein fibrillin-1. Marfan syndrome affects most organs and tissues, especially the skeleton, lungs, eyes, heart, and the large blood vessel that distributes blood from the heart to the rest of the body. A case report of Marfan syndrome has been reported with oral features. The dental problems of the child were treated under general anesthesia and a one-month review showed intact stainless steel crowns' restorations and no signs of secondary caries. |
url |
http://dx.doi.org/10.1155/2012/595343 |
work_keys_str_mv |
AT rajendranganesh marfansyndromeacasereport AT rajendranvijayakumar marfansyndromeacasereport AT haridossselvakumar marfansyndromeacasereport |
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