Document Detail


Dentin dysplasia type I--a case report.
MedLine Citation:
PMID:  10081578     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
A case report on dentin dysplasia type I, a congenital disease (autosomal dominant gene defect) affecting deciduous and permanent teeth, is depicted including representations of clinical and histological features, X-ray and CT-findings. Therapy includes extraction of all teeth, ectomization of cystic alteration, revision of paranasal sinus. Aesthetic and functional rehabilitation by means of insertion of a complete denture was achieved.
Authors:
F Neumann; F Würfel; T Mundt
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Annals of anatomy = Anatomischer Anzeiger : official organ of the Anatomische Gesellschaft     Volume:  181     ISSN:  0940-9602     ISO Abbreviation:  Ann. Anat.     Publication Date:  1999 Jan 
Date Detail:
Created Date:  1999-04-20     Completed Date:  1999-04-20     Revised Date:  2005-05-18    
Medline Journal Info:
Nlm Unique ID:  100963897     Medline TA:  Ann Anat     Country:  GERMANY    
Other Details:
Languages:  eng     Pagination:  138-40     Citation Subset:  IM    
Affiliation:
Department of Oral and Maxillofacial Surgery/Plastic Operations, Ernst Moritz Arndt University, Greifswald, Germany.
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MeSH Terms
Descriptor/Qualifier:
Adult
Dentin Dysplasia / genetics,  pathology*,  radiography,  surgery
Female
Genes, Dominant
Humans
Male
Pedigree
Tomography, X-Ray Computed

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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