Rendu-Osler-Weber syndrome: A family investigation and review
Rendu-Osler-Weber syndrome is a rare genetic condition characterized by mucocutaneous and visceral fibrovascular dysplasia leading to multiple macular or papular vascular lesions of skin, mucosal surfaces and occasionally viscera that show tendency towards hemorrhage. The orofacial features of the c...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
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Wolters Kluwer Medknow Publications
2009-01-01
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| Series: | Journal of Indian Academy of Oral Medicine and Radiology |
| Subjects: | |
| Online Access: | http://www.jiaomr.in/article.asp?issn=0972-1363;year=2009;volume=21;issue=2;spage=83;epage=88;aulast=Mahima |
| _version_ | 1818062717555048448 |
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| author | V G Mahima Karthikeya Patil Madhur Kapoor Shalini Kalia |
| author_facet | V G Mahima Karthikeya Patil Madhur Kapoor Shalini Kalia |
| author_sort | V G Mahima |
| collection | DOAJ |
| description | Rendu-Osler-Weber syndrome is a rare genetic condition characterized by mucocutaneous and visceral fibrovascular dysplasia leading to multiple macular or papular vascular lesions of skin, mucosal surfaces and occasionally viscera that show tendency towards hemorrhage. The orofacial features of the condition in an affected family and in particular a 33-year-old Indian male patient, are illustrated along with summarization of management aspects in a dental setup. |
| first_indexed | 2024-12-10T14:08:39Z |
| format | Article |
| id | doaj.art-47d5c2d8fdf54d8a9e42c77aa22c4cad |
| institution | Directory Open Access Journal |
| issn | 0972-1363 0975-1572 |
| language | English |
| last_indexed | 2024-12-10T14:08:39Z |
| publishDate | 2009-01-01 |
| publisher | Wolters Kluwer Medknow Publications |
| record_format | Article |
| series | Journal of Indian Academy of Oral Medicine and Radiology |
| spelling | doaj.art-47d5c2d8fdf54d8a9e42c77aa22c4cad2022-12-22T01:45:35ZengWolters Kluwer Medknow PublicationsJournal of Indian Academy of Oral Medicine and Radiology0972-13630975-15722009-01-01212838810.4103/0972-1363.57894Rendu-Osler-Weber syndrome: A family investigation and reviewV G MahimaKarthikeya PatilMadhur KapoorShalini KaliaRendu-Osler-Weber syndrome is a rare genetic condition characterized by mucocutaneous and visceral fibrovascular dysplasia leading to multiple macular or papular vascular lesions of skin, mucosal surfaces and occasionally viscera that show tendency towards hemorrhage. The orofacial features of the condition in an affected family and in particular a 33-year-old Indian male patient, are illustrated along with summarization of management aspects in a dental setup.http://www.jiaomr.in/article.asp?issn=0972-1363;year=2009;volume=21;issue=2;spage=83;epage=88;aulast=MahimaHereditary hemorrhagic telangiectasiaepistaxisgastrointestinal bleedingoral petechiaeRendu-Osler-Weber syndrome |
| spellingShingle | V G Mahima Karthikeya Patil Madhur Kapoor Shalini Kalia Rendu-Osler-Weber syndrome: A family investigation and review Journal of Indian Academy of Oral Medicine and Radiology Hereditary hemorrhagic telangiectasia epistaxis gastrointestinal bleeding oral petechiae Rendu-Osler-Weber syndrome |
| title | Rendu-Osler-Weber syndrome: A family investigation and review |
| title_full | Rendu-Osler-Weber syndrome: A family investigation and review |
| title_fullStr | Rendu-Osler-Weber syndrome: A family investigation and review |
| title_full_unstemmed | Rendu-Osler-Weber syndrome: A family investigation and review |
| title_short | Rendu-Osler-Weber syndrome: A family investigation and review |
| title_sort | rendu osler weber syndrome a family investigation and review |
| topic | Hereditary hemorrhagic telangiectasia epistaxis gastrointestinal bleeding oral petechiae Rendu-Osler-Weber syndrome |
| url | http://www.jiaomr.in/article.asp?issn=0972-1363;year=2009;volume=21;issue=2;spage=83;epage=88;aulast=Mahima |
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