scholarly journals Primary Fused Teeth and Findings in Permanent Dentition

2018 ◽  
Vol 27 (2) ◽  
pp. 129-132
Author(s):  
Hatice Açıkel ◽  
Sevgin İbiş ◽  
Emine Şen Tunç
Keyword(s):  
Permanent Tooth ◽  
Permanent Dentition ◽  
Dental Anomalies ◽  
Turkish Children ◽  
Clinical Complications ◽  
Ectopic Eruption ◽  
Fused Teeth ◽  
The Mean ◽  
Dental Records

Objective: The aim of this study was to investigate the characteristics of primary fused teeth (PFT) and their effect on permanent dentition in a group of Turkish children. Subjects and Methods: Dental records of 13,450 pediatric patients who attended the Pediatric Dental Clinic in northern Turkey between 2015 and 2017 were reviewed. Forty patients had been diagnosed with PFT and were included in the study. Clinical and radiographic examinations were conducted, and the distribution of PFT was calculated by type, sex, affected jaw, associated dental anomalies, and clinical complications. Data analysis involved descriptive statistics. Results: A total of 50 PFT were detected in the 40 patients. The mean age of patients was 6.7 ± 0.3 years (range 3–10 years). The most common PFT were the mandibular lateral incisors and canines (34, 68%). The most prevalent type of PFT was type III (20, 40%). Of the 40 patients with PFT, 34 (85%) also ex­hibited other dental anomalies such as tooth aplasia, peg-shaped incisors, talon cusps, ectopic eruption, and delayed eruption in both related and unrelated areas. The most common complications of PFT were fusion-related tooth aplasia (n = 26 [76%]) and caries formation in the affected teeth (24 [48%]). Conclusion: In this study, PFT were frequently observed in the mandibular anterior region. Caries formation and dental anomalies, especially permanent tooth aplasia, were often encountered in areas where PFT were seen. Hence, parents should be informed about possible dental problems associated with PFT and be encouraged to schedule regular follow-up appointments.

scholarly journals Flow diverter stents in the treatment of recanalized intracranial aneurysms

2021 ◽  
pp. 159101992199050
Author(s):  
Erol Akgul ◽  
Hasan Bilen Onan ◽  
Irem Islek ◽  
Mehmet Tonge ◽  
Yavuz Durmus ◽  
...  
Keyword(s):  
Intracranial Aneurysms ◽  
Demographic Data ◽  
Previous Treatment ◽  
Flow Diverter ◽  
Serious Adverse Events ◽  
Clinical Complications ◽  
Tertiary Hospitals ◽  
The Mean ◽  
Technical Complication

Background We assessed the safety and efficacy of flow diverter stents (FDSs) in the treatment of recanalized or residual intracranial aneurysms treated endovascularly. Materials & Methods Patients whose recanalized or residual aneurysms were treated with FDSs in five tertiary hospitals were reviewed retrospectively. The patients’ demographic data, aneurysm characteristics, types of previous treatment, and clinical complications, or serious adverse events associated with FDSs, as well as the results of neurological and angiographic follow-up assessments, were recorded. Results Eighty-six patients (37 males) with 87 aneurysms were included in this study. Eighty (91.9%) aneurysms were in the anterior and seven (8.1%) in the posterior circulation. The initial treatment methods were the primary coiling or balloon remodeling technique in 69 (79.3%) and stent-assisted coiling in 18 (20.7%) aneurysms. The endovascular procedure was successful in all patients. Complications occurred in four patients, for a total complication rate of 4.6%. A technical complication developed in one patient (1.2%). An in-stent thrombosis treated with tirofiban was seen in two cases. Late in-stent stenosis exceeding 50% was treated with balloon angioplasty in one patient. The mean length of follow-up was 21.0 months. The first angiographic follow-up (3–6 months) revealed the complete occlusion of 74 aneurysms (85.1%). While 76 aneurysms (87.4%) were occluded at the last angiographic follow-up (mean: 26.0 months), 11 aneurysms (12.6%) were still filling. Morbimortality was zero. Conclusion The drawback of endovascular treatment is aneurysmal remnants or recurrences, which is safely and durably amenable to flow diversion.

A European multicentric experience using the CardioSEAL® and Starflex double umbrella devices to close interatrial communications holes within the oval fossa

2000 ◽  
Vol 10 (5) ◽  
pp. 519-526 ◽  
Author(s):  
M. Carminati ◽  
S. Giusti ◽  
G. Hausdorf ◽  
S. Qureshi ◽  
M. Tynan ◽  
...  
Keyword(s):  
General Anesthesia ◽  
Surgical Repair ◽  
Clinical Success ◽  
The Other ◽  
Thromboembolic Events ◽  
Clinical Complications ◽  
The Mean ◽  
One Year ◽  
Flap Valve

AbstractIn this review, we describe the experience from 13 European centres using the CardioSEAL and Starflex double umbrella devices to close interatrial communications within the oval fossa (so-called ‘stcundum’ defects). Between October 1996 and April 1999, the procedure was attempted in 334 patients with a mean age of 12 years and a mean weight of 44kg. The mean measured stretched diameter of the defect was 15 mm. In the overall group, the defect was solitary in 245 patients (73%), multiple in 21 (6%), associated with an aneurysm of the flap valve in 15 (5%), was represented by patency of the oval foramen in 44 (13%), and was a fenestration in a Fontan repair in 9 (3%). In all patients, the devices were inserted under general anesthesia, using fluoroscopic and transesophageal echocardiographic control. Implantation was achieved in 325 (97,3%). The device embolized within either a few minutes or a few hours in 13 patients (4%). Of these, uncomplicated surgical repair was undertaken in 10, while the device was retrieved in 3 using catheters and a second device was successfully implanted. Residual shunting was detected immediately after the procedure in 41% of the patients, with the incidence decreasing to 31% at discharge, 24% at 1 month, 21% at 6 months, and 20.5% at one year. During the period of follow-up, elective surgical repair became necessary in two patients, due to malposition of the device in one, and late embolization in the other. Fractures of arms were seen in 6.1%, most commonly with the largest devices. All those with fractured arms of the device were asymptomatic, and no clinical complications related to the fractures were observed. There were no arrythmias, endocarditis, valvar distortion, thromboembolic events, or other complications. After one year of follow-up, clinical success, defined as complete closure of the defect or presence of only a trivial leak, had been obtained in 92.5% of the patients. We conclude, therefore, that these devices produce excellent results when used to close defects of small to moderate size. Results are less than optimal, or else complications ensure, when attempts are made to close very large defects.

scholarly journals Dental anomalies in children with cleft lip and palate in Western Australia

2016 ◽  
Vol 10 (02) ◽  
pp. 254-258 ◽  
Author(s):  
Wendy Nicholls
Keyword(s):  
Western Australia ◽  
Cleft Lip ◽  
Cleft Lip And Palate ◽  
X Rays ◽  
Dental Anomalies ◽  
Dental Patients ◽  
Bilateral Cleft Lip ◽  
Males And Females ◽  
The Mean ◽  
Dental Records

ABSTRACT Objective: The purpose of this paper was to describe the prevalence and type of dental anomalies in the primary and permanent dentition in children with a cleft condition at Princess Margaret Hospital in Perth, Western Australia. Materials and Methods: The details of 162 current dental patients extracted from the main dental database through their year of birth for the period 1998–2001 were selected consecutively. Dental records and X-rays were examined by one examiner (WN) and verified by a second examiner (RB) to determine dental development. The mean age of the subjects was 10.8 years with equal numbers of males and females. Subjects were further divided into cleft type; unilateral cleft lip (UCL) and palate, bilateral cleft lip (BCL) and palate, UCL, BCL, and cleft palate. Results: One hundred sixty-two subjects were grouped into 21 categories of anomaly or abnormality. Prevalence rates for the categories were calculated for the overall group and for gender and cleft type. Conclusion: Overall, 94% of patients were found to have at least one dental anomaly, with fifty-six (34%) patients having more than one anomaly or abnormality.

scholarly journals Bilateral fusion of permanent canine and lateral incisor

1970 ◽  
Vol 9 (2) ◽  
pp. 122-124
Author(s):  
VP Singh ◽  
S Dhital ◽  
TP Shankar Babu ◽  
M Agarwal
Keyword(s):  
Case Report ◽  
Permanent Dentition ◽  
Primary Dentition ◽  
Lateral Incisor ◽  
Dental Anomalies ◽  
Number Of Teeth ◽  
Fused Teeth ◽  
Tooth Buds ◽  
Fused Tooth

Fusion is described as the union of two or more tooth buds. It is characterized by a reduced number of teeth , when fused tooth is counted as one . The prevalence of fused teeth in primary dentition is below 1% and even more less in permanent dentition. The occurrence of fusion in primary dentition may be followed by dental anomalies in permanent dentition. This case report presents a case of bilateral fusion of lateral incisor and canine in primary dentition which was followed by similar fusion in permanent dentition. The aim of this report is to highlight the rarity of such condition by virtue of the number of such cases reported in literature and to evaluate their pulpal morphologies to understand the type of fusion and presence of any other associated pathologies. Keywords: dental anamoly; fusion; gemination DOI: http://dx.doi.org/10.3126/hren.v9i2.4987 Health Renaissance 2011: Vol.9 (No.2): 122-124

scholarly journals Fused primary first mandibular macromolar with a unique relation to its permanent successors: A rare tooth anomaly

2013 ◽  
Vol 07 (02) ◽  
pp. 239-242 ◽  
Author(s):  
Abhishek Dhindsa ◽  
Shalini Garg ◽  
S. G. Damle ◽  
Shireen Opal ◽  
Tavleen Singh
Keyword(s):  
Permanent Tooth ◽  
Permanent Dentition ◽  
Dental Anomalies ◽  
Supernumerary Tooth ◽  
Deciduous Dentition ◽  
Primary Molar ◽  
Anterior Teeth ◽  
Mandibular First Premolar ◽  
Double Teeth ◽  
Fused Tooth

ABSTRACTDental anomalies of number and forms may occur in the primary and permanent dentition. Various terms have been used to describe dental twinning anomalies: Germination, fusion, concrescence, double teeth, conjoined teeth, twinned teeth, geminifusion, and vicinifusion. Fused tooth is a developmental anomaly that is seen more frequently in the primary than the permanent dentition. Double tooth involving deciduous anterior teeth is found mostly in the mandible.Very few cases of nonsyndromic double primary molar have been reported in the literature. The succeeding permanent tooth is often found missing congenitally in the same region. This article reports a very rare unilateral occurrence of an anomalous, primary mandibular first macromolar formed by fusion with a dysmorphic premolar like supernumerary tooth in deciduous dentition period. Instead of agenesis of succedaneous tooth, the double tooth has been succeeded by normally developing mandibular first premolar in the same region.

scholarly journals The Prevalence of Dental Anomalies in Orthodontic Patients at the State University of New York at Buffalo

2013 ◽  
Vol 14 (3) ◽  
pp. 518-523 ◽  
Author(s):  
Athari Al-Amiri ◽  
Sawsan Tabbaa ◽  
Charles Brian Preston ◽  
Thikriat Al-Jewair
Keyword(s):  
New York ◽  
Permanent Tooth ◽  
The State ◽  
State University ◽  
Dental Anomalies ◽  
Inclusion Criteria ◽  
Supernumerary Teeth ◽  
Lateral Cephalograms ◽  
Orthodontic Patients ◽  
The Mean

ABSTRACT Objective To determine the prevalence of permanent tooth anomalies in patients attending the graduate orthodontic clinic at the State University of New York at Buffalo. Materials and methods Charts of 496 subjects (310 females and 186 males) met the inclusion criteria for this study. The mean ages were 16 years and 3 months for the combined gender sample that received orthodontic treatment in the graduate orthodontic clinic between 2007 and 2010. Full pretreatment records (intraoral photographs, digital study models, lateral cephalograms and panoramic radiographs) were used for the assessment. Charts were examined for these anomalies: agenesis, supernumerary, impaction and delayed tooth eruption. Subjects were categorized by gender and ethnicity. The percentages of the anomalies were assessed according to type of malocclusion, gender, race, location, tooth class and region in the dental arches. Results Sixty-four subjects (12.9%) had at least one occurrence of delayed eruption and impaction (DEI), followed by 47 subjects (9.5%) who had at least one occurrence of agenesis, and seven (1.4%) had a supernumerary condition. Approximately 80% of the subjects had no dental anomalies. The presence of more than one anomaly was observed in 61 subjects. Twelve subjects (2.4%) had both agenesis and DEI. Agenesis tended to be more common in class II malocclusions (p = 0.012). Conclusion The prevalence of permanent tooth anomalies was (20.4%). The percentage occurrence of DEI was the highest (12.9%) followed by dental agenesis (9.5%) and supernumerary teeth (1.4%) in the orthodontic patients at the State University of New York at Buffalo. How to cite this article Al-Amiri A, Tabbaa S, Preston CB, Al-Jewair T. The Prevalence of Dental Anomalies in Orthodontic Patients at the State University of New York at Buffalo. J Contemp Dent Pract 2013;14(3):518-523.

scholarly journals Fusion or Gemination? Diagnosis and Management in Primary Teeth: A Report of Two Cases

2021 ◽  
Vol 2021 ◽  
pp. 1-6
Author(s):  
Mouna Ben Salem ◽  
Farah Chouchene ◽  
Fatma Masmoudi ◽  
Ahlem Baaziz ◽  
Fethi Maatouk ◽  
...  
Keyword(s):  
Dental Caries ◽  
Primary Teeth ◽  
Treatment Plan ◽  
Multidisciplinary Treatment ◽  
Lateral Incisor ◽  
Dental Anomalies ◽  
Developmental Abnormalities ◽  
Clinical Complications ◽  
First Case ◽  
Fused Teeth

Primary double teeth (PDT), referring to either gemination or fusion, are one of the most important and frequent developmental dental anomalies that can affect children’s oral health. Many clinical complications are correlated with these anomalies, such as dental caries, malocclusions, periodontal problems, and dental anomalies in permanent dentition. The aim of this report was to describe, through two cases, a case of gemination and another of fusion, the clinical management, the consequent effects, and the possible repercussions of these two developmental abnormalities on permanent successors. The first case involved gemination of the primary maxillary left central incisor (#61) in a 6-year-old boy. The patient presented with dental caries in the geminated tooth and its contiguous primary left lateral incisor (#62). The radiological examination revealed a slight developmental delay in the permanent left lateral incisor (#22). The treatment plan involved performing a pulpotomy and restoring the dental crowns of the affected teeth. The second clinical case describes a 6-year-old girl with unilateral fusion between a primary mandibular lateral incisor (#72) and a supernumerary tooth (#72’). The treatment included restoration of the deep grooves of the fused teeth using flowable composite and coronal restoration of the contiguous left primary canine (#73). Clinical and radiological follow-ups were performed every 3 months to monitor the development of teeth. No clinical and radiological symptoms were noted during the follow-up visits. PDT may require a multidisciplinary treatment. They should be diagnosed early to avoid and treat any possible complications in both the primary teeth and their permanent successors.

scholarly journals Tooth Triplet: A Rare Case Report

2009 ◽  
Vol 3 (1) ◽  
pp. 3-5
Author(s):  
Samir Dutta ◽  
Puneet Goenka
Keyword(s):  
Rare Case ◽  
Histological Section ◽  
Permanent Tooth ◽  
Deciduous Teeth ◽  
Supernumerary Tooth ◽  
Rare Case Report ◽  
Long Term Follow Up ◽  
Fused Teeth

ABSTRACT A rare case of fusion of two deciduous teeth with a supernumerary tooth is reported. The fused teeth were causing deviation of the path of eruption of the permanent tooth. Thus extraction was planned for them. The histological section of the extracted tooth confirmed the phenomenon of fusion. Long term follow up showed normal eruption of the permanent tooth there after.

Canadian Registry of LVIS Jr for Treatment of Intracranial Aneurysms (CaRLA)

2016 ◽  
Vol 9 (9) ◽  
pp. 849-853 ◽  
Author(s):  
Jai Jai Shiva Shankar ◽  
Aiman Quateen ◽  
Alain Weill ◽  
Donatella Tampieri ◽  
Maria Del Pilar Cortes ◽  
...  
Keyword(s):  
Intracranial Aneurysms ◽  
Neurological Complications ◽  
Neurological Deficits ◽  
Maximum Diameter ◽  
Class Iii ◽  
Clinical Complications ◽  
Low Profile ◽  
The Mean ◽  
Age Range

IntroductionStents reduce the rate of angiographic recurrence of intracranial aneurysms. The newest stent for intracranial use is the Low-profile Visible Intraluminal Support device (LVIS Jr).ObjectiveTo assess the efficacy of the new stent in a multicenter retrospective registry.Materials and methodCenters across Canada using LVIS Jr were contacted and asked to participate in a retrospective registry of consecutive patients treated with LVIS Jr for intracranial aneurysms between January 2013 and July 2015.ResultsA total of 102 patients, with saccular aneurysms in 100 patients (72 women; age range 21–78 years; mean 56.0 years; median 57.5 years) were treated with a LVIS Jr stent. The mean maximum diameter of the dome and neck of the aneurysm and dome to neck ratios were 8.3 mm±7.7 mm, 4.4 mm±1.9 mm, and 1.86±1.22, respectively. Angiographic complications arose in 23 patients, clinical complications in 9 patients, and only 3% of permanent neurological deficits occurred. Death occurred in 1 patient, unrelated to the stent. The ruptured status of the aneurysms (OR=3.29; p=0.046) and use of LVIS Jr for bailout (OR=2.54; p=0.053) showed a trend towards significant association with higher angiographic complications. At the last available follow-up, 68 class I, 20 class II, and 12 class III results were seen.ConclusionsThe LVIS Jr stent is a safe and effective device for stent-assisted coiling, with 3% permanent neurological complications. Stent-assisted coiling continues to be technically challenging in cases of ruptured aneurysms and bailout situations.

Sound Production Treatment for Acquired Apraxia of Speech: An Examination of Dosage in Relation to Probe Performance

2020 ◽  
pp. 1-16
Author(s):  
Julie L. Wambaugh ◽  
Lydia Kallhoff ◽  
Christina Nessler
Keyword(s):  
Retrospective Analysis ◽  
Sound Production ◽  
Apraxia Of Speech ◽  
Practice Schedule ◽  
Practice Schedules ◽  
Baseline Performance ◽  
The Mean ◽  
Number Of Treatment ◽  
The Impact

Purpose This study was designed to examine the association of dosage and effects of Sound Production Treatment (SPT) for acquired apraxia of speech. Method Treatment logs and probe data from 20 speakers with apraxia of speech and aphasia were submitted to a retrospective analysis. The number of treatment sessions and teaching episodes was examined relative to (a) change in articulation accuracy above baseline performance, (b) mastery of production, and (c) maintenance. The impact of practice schedule (SPT-Blocked vs. SPT-Random) was also examined. Results The average number of treatment sessions conducted prior to change was 5.4 for SPT-Blocked and 3.9 for SPT-Random. The mean number of teaching episodes preceding change was 334 for SPT-Blocked and 179 for SPT-Random. Mastery occurred within an average of 13.7 sessions (1,252 teaching episodes) and 12.4 sessions (1,082 teaching episodes) for SPT-Blocked and SPT-Random, respectively. Comparisons of dosage metric values across practice schedules did not reveal substantial differences. Significant negative correlations were found between follow-up probe performance and the dosage metrics. Conclusions Only a few treatment sessions were needed to achieve initial positive changes in articulation, with mastery occurring within 12–14 sessions for the majority of participants. Earlier occurrence of change or mastery was associated with better follow-up performance. Supplemental Material https://doi.org/10.23641/asha.12592190

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