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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| Format: | Book |
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Hindawi Limited,
2012-01-01T00:00:00Z.
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| 042 | |a dc | ||
| 100 | 1 | 0 | |a Rajendran Ganesh |e author |
| 700 | 1 | 0 | |a Rajendran Vijayakumar |e author |
| 700 | 1 | 0 | |a Haridoss Selvakumar |e author |
| 245 | 0 | 0 | |a Marfan Syndrome: A Case Report |
| 260 | |b Hindawi Limited, |c 2012-01-01T00:00:00Z. | ||
| 500 | |a 2090-6447 | ||
| 500 | |a 2090-6455 | ||
| 500 | |a 10.1155/2012/595343 | ||
| 520 | |a 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. | ||
| 546 | |a EN | ||
| 690 | |a Dentistry | ||
| 690 | |a RK1-715 | ||
| 655 | 7 | |a article |2 local | |
| 786 | 0 | |n Case Reports in Dentistry, Vol 2012 (2012) | |
| 787 | 0 | |n http://dx.doi.org/10.1155/2012/595343 | |
| 787 | 0 | |n https://doaj.org/toc/2090-6447 | |
| 787 | 0 | |n https://doaj.org/toc/2090-6455 | |
| 856 | 4 | 1 | |u https://doaj.org/article/9f9d4051e23d4f0d9dbe6fd6bd61bfc7 |z Connect to this object online. |