| Literature DB >> 10081578 |
F Neumann1, F Würfel, T Mundt.
Abstract
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.Entities:
Mesh:
Year: 1999 PMID: 10081578 DOI: 10.1016/S0940-9602(99)80120-4
Source DB: PubMed Journal: Ann Anat ISSN: 0940-9602 Impact factor: 2.698