| Dentinogenesis imperfecta: a review and case report of a family over four generations. | |
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MedLine Citation:
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PMID: 19075443 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Dentinogenesis imperfecta (DGI) is one of the most common hereditary disorders of dentin formation. It follows an autosomal dominant pattern of transmission, affecting both the formation and mineralization of dentin. Either or both primary and permanent dentition is affected by it. This paper briefly reviews the manifestations of DGI Type II (DGI1) and presents a case report of a family affected with DGI1 over four generations. |
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Authors:
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Sudhir Bhandari; Karneev Pannu |
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Publication Detail:
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Type: Case Reports; Journal Article; Review |
Journal Detail:
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Title: Indian journal of dental research : official publication of Indian Society for Dental Research Volume: 19 ISSN: 0970-9290 ISO Abbreviation: Indian J Dent Res Publication Date: 2008 Oct-Dec |
Date Detail:
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Created Date: 2008-12-16 Completed Date: 2009-03-31 Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 9202990 Medline TA: Indian J Dent Res Country: India |
Other Details:
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Languages: eng Pagination: 357-61 Citation Subset: D |
Affiliation:
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Department of Prosthodontics, HSJ Institute of Dental Sciences and Hospital, Panjab University, Chandigarh, India. drsudhirbhandari@yahoo.co.in |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Adolescent Dental Pulp / abnormalities Dentin / abnormalities Dentinogenesis Imperfecta / genetics* Female Follow-Up Studies Genes, Dominant / genetics Humans Male Pedigree Radiography, Panoramic Tooth Attrition / genetics Tooth Discoloration / genetics Young Adult |
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