Osteogenesis imperfecta and dentinogenesis imperfecta: Clinical features and dental management
Osteogenesis imperfecta (OI) is a rare congenital condition, marked by fragile bones, skeletal deformities and additional extra-skeletal symptoms. Depending upon the degree of seriousness, affected people can either carry on with a mostly unrestricted, independent life, or their mobility is severely...
Main Authors: | , , , |
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Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Medknow Publications
2022-01-01
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Series: | Current Medicine Research and Practice |
Subjects: | |
Online Access: | http://www.cmrpjournal.org/article.asp?issn=2352-0817;year=2022;volume=12;issue=4;spage=167;epage=172;aulast=Grover |