Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
1.
Rom J Morphol Embryol ; 60(4): 1285-1290, 2019.
Article in English | MEDLINE | ID: mdl-32239106

ABSTRACT

INTRODUCTION: Untreated middle mesial canals (MMCs) of mandibular permanent molars can result in endodontic treatment failure. AIM: The aim of this retrospective study was to investigate the incidence of MMC of mandibular molars in a Romanian population. PATIENTS, MATERIALS AND METHODS: In total, there were evaluated 144 mandibular first permanent molars and 140 mandibular second permanent molars by using cone-beam computed tomography (CBCT) scans. RESULTS: The MMC was identified in 5.67% of mandibular first permanent molars, respectively in 4.28% of mandibular second permanent molars. The male∕female ratio of MMC presence was 1:3 of mandibular first molars and inverted for mandibular second molars (5:1). The presence of MMC in mandibular first molars was associated in all cases of our study with a second distal canal, unlike the mandibular second molars where no second distal canal was associated with a MMC. CONCLUSIONS: In Romanian population, the MMC of mandibular first molars, when present, is commonly associated with a second distal canal, unlike the mandibular second molars where the occurrence of a MMC was associated with only one distal canal. When performing the preoperative evaluation, it has also to be considered the patient gender, since the male∕female ratio of MMC was 1:3 in mandibular first molars and 5:1 in mandibular second molars.


Subject(s)
Cone-Beam Computed Tomography , Dental Pulp Cavity/diagnostic imaging , Mandible/diagnostic imaging , Molar/diagnostic imaging , Dental Pulp Cavity/surgery , Female , Humans , Incidence , Male , Mandible/surgery , Molar/surgery , Romania
2.
Rom J Morphol Embryol ; 59(1): 359-365, 2018.
Article in English | MEDLINE | ID: mdl-29940650

ABSTRACT

According to their phenotypic features, the hereditary dentin defects in humans are categorized in two major classes: dentinogenesis imperfecta and dentin dysplasia. At its turn, the dentin dysplasia is subdivided in dentin dysplasia type I and dentin dysplasia type II, a milder clinical manifestation of the condition. Here we report the clinical and radiographic findings of dentin dysplasia type II in two members of a family, a young adult female and her mother. Except a mild shade change of the incisal margins in upper central incisors and left upper canine of the daughter no abnormal occlusal wear or crown shape change of the teeth were disclosed in both patients. However, confluent large pulp stones in the thistle-tube shaped pulp chambers and pulpal obliteration were a common finding. The condition was diagnosed as dentin dysplasia type II.


Subject(s)
Dentin Dysplasia/diagnosis , Adult , Dentin Dysplasia/pathology , Female , Humans , Rare Diseases , Young Adult
3.
Rev Med Chir Soc Med Nat Iasi ; 114(4): 1175-7, 2010.
Article in Romanian | MEDLINE | ID: mdl-21500475

ABSTRACT

If, not long time ago, the simple prosthetic rehabilitation of an edentulous patient--with or without additional maxillary teeth abnormalities--was the only therapeutic solution, presently, the pre-prosthetic orthodontic treatment enabling the dental restoration treatment meets the basic requirements of any dental treatment, i.e. the (re)set-up of the morphological and functional integrity and the functions of jaws, with minimum biological sacrifice.


Subject(s)
Dental Restoration, Permanent/methods , Interdisciplinary Communication , Jaw, Edentulous, Partially/rehabilitation , Occlusal Adjustment , Oral Surgical Procedures, Preprosthetic , Humans , Jaw, Edentulous/rehabilitation , Osteotomy
SELECTION OF CITATIONS
SEARCH DETAIL
...