An integrated treatment approach: a case report for dentinogenesis imperfecta type II.

dc.contributor.authorShetty, Nen_US
dc.contributor.authorJoseph, Men_US
dc.contributor.authorBasnet, Pen_US
dc.contributor.authorDixit, Sen_US
dc.date.accessioned2009-05-28T04:13:23Z
dc.date.available2009-05-28T04:13:23Z
dc.date.issued2007-04-08en_US
dc.descriptionKathmandu University Medical Journal.en_US
dc.description.abstractDentinogenesis imperfecta type II or hereditary opalscent dentin is one of the most common autosomal dominant anomaly of dentin that occurs in both sex affecting approximately 1:8000 persons. Clinically this disorder is characterized by variable blue gray to yellow brown teeth, with fracture of enamel and excessive wear. The treatment strategy is focused towards protecting teeth from further wear and tear and total oral rehabilitation of patient with paramount importance to aesthetics, obtaining an appropriate vertical dimension and providing soft tissue support which will help to return the facial profile to a more normal appearance. A multidisciplinary treatment planning is required for treatment of these individuals.en_US
dc.description.affiliationDepartment of Conservative Dentistry and Endodontics, Manipal college of Dental Science, Mangalore, Karnataka. India. neetaraj92@rediffmail.comen_US
dc.identifier.citationShetty N, Joseph M, Basnet P, Dixit S. An integrated treatment approach: a case report for dentinogenesis imperfecta type II. Kathmandu University Medical Journal. 2007 Apr-Jun; 5(2): 230-3en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/46621
dc.language.isoengen_US
dc.source.urihttps://www.kumj.com.npen_US
dc.source.urihttps://kumj.com.np/ftp/issue/18/230-233-An-Integrated-treatment-approach-A-Case-Report%20.pdfen_US
dc.titleAn integrated treatment approach: a case report for dentinogenesis imperfecta type II.en_US
dc.typeJournal Articleen_US
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