Capdepont's Teeth - a Hereditary Dentin Defect: Case Report & Review

Capdepont's Teeth - a Hereditary Dentin Defect: Case Report & Review

Dentinogenesis imperfecta is an autosomal dominant genetic disorder with abnormal dentin structure affecting both primary and permanent dentitions leading to discolouration and attrition of teeth. Diagnosis is usually based on family history, a detailed clinical examination and pedigree construction...

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Main Authors: Pai,Anuradha, Prasad R,Shesha, Ramakrishna, Rao,Raghoothama
Language:English
Published: Universidad de La Frontera. Facultad de Medicina 2012
Subjects:
discolouration
attrition
dentin defect
Online Access:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0718-381X2012000200018
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spelling oai:scielo:S0718-381X20120002000182012-11-09Capdepont's Teeth - a Hereditary Dentin Defect: Case Report & ReviewPai,AnuradhaPrasad R,SheshaRamakrishna,Rao,Raghoothama discolouration attrition dentin defect Dentinogenesis imperfecta is an autosomal dominant genetic disorder with abnormal dentin structure affecting both primary and permanent dentitions leading to discolouration and attrition of teeth. Diagnosis is usually based on family history, a detailed clinical examination and pedigree construction. Treatment involves preservation of teeth, removal of infection, restoration of function and esthetics.info:eu-repo/semantics/openAccessUniversidad de La Frontera. Facultad de MedicinaInternational journal of odontostomatology v.6 n.2 20122012-08-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0718-381X2012000200018en10.4067/S0718-381X2012000200018
institution Scielo Chile
collection Scielo Chile
language English
topic discolouration
attrition
dentin defect
spellingShingle discolouration
attrition
dentin defect
Pai,Anuradha
Prasad R,Shesha
Ramakrishna,
Rao,Raghoothama
Capdepont's Teeth - a Hereditary Dentin Defect: Case Report & Review
description Dentinogenesis imperfecta is an autosomal dominant genetic disorder with abnormal dentin structure affecting both primary and permanent dentitions leading to discolouration and attrition of teeth. Diagnosis is usually based on family history, a detailed clinical examination and pedigree construction. Treatment involves preservation of teeth, removal of infection, restoration of function and esthetics.
author Pai,Anuradha
Prasad R,Shesha
Ramakrishna,
Rao,Raghoothama
author_facet Pai,Anuradha
Prasad R,Shesha
Ramakrishna,
Rao,Raghoothama
author_sort Pai,Anuradha
title Capdepont's Teeth - a Hereditary Dentin Defect: Case Report & Review
title_short Capdepont's Teeth - a Hereditary Dentin Defect: Case Report & Review
title_full Capdepont's Teeth - a Hereditary Dentin Defect: Case Report & Review
title_fullStr Capdepont's Teeth - a Hereditary Dentin Defect: Case Report & Review
title_full_unstemmed Capdepont's Teeth - a Hereditary Dentin Defect: Case Report & Review
title_sort capdepont's teeth - a hereditary dentin defect: case report & review
publisher Universidad de La Frontera. Facultad de Medicina
publishDate 2012
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0718-381X2012000200018
work_keys_str_mv AT paianuradha capdepontsteethahereditarydentindefectcasereportampreview
AT prasadrshesha capdepontsteethahereditarydentindefectcasereportampreview
AT ramakrishna capdepontsteethahereditarydentindefectcasereportampreview
AT raoraghoothama capdepontsteethahereditarydentindefectcasereportampreview
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