The Frequency and Characteristics of Mesiodens in a Turkish Patient Population

نویسندگان

  • Fatih Kazanci
  • Mevlut Celikoglu
  • Ozkan Miloglu
  • Hanifi Yildirim
  • Ismail Ceylan
چکیده

OBJECTIVES The aim of this study was to investigate the frequency and characteristics of mesiodens among a group of orthodontic patients in Turkey. METHODS A retrospective study was performed using panoramic radiographs of 3,351 patients ranging in age from 8 to 16 subjected to dental treatment in the Department of Oral and Maxillofacial Radiology and Department of Orthodontics (Erzurum, Turkey) between 1996 and 2008. All medical and demographic data (age and sex) were obtained from the files. Descriptive characteristics of mesiodentes, including number, shape, position, complication caused by mesiodens and treatment were recorded. The Chi-squared test was used. RESULTS Results show that the frequency of mesiodens was 0.3% with the ratio of boys (6 cases) to girls (4 cases) being 1.5:1 and this was not statistically significant (P>.05). Of the 10 children, 8 (80.0%) had 1 mesiodens and 2 (20.0%) had 2 mesiodentes bilaterally to midline. Of the 12 mesiodentes, 8 (66.7%) were fully impacted, 7 (58.3%) in a vertical position and 9 (75.0%) conical shape. The most common complication caused by mesiodens was delayed eruption of the permanent incisors in 4 cases (40.0%). CONCLUSIONS The frequency of mesiodens in Turkish orthodontic patients was found to be 0.3% and more frequently in males with the ratio being approximately 1.5:1. Most of the mesiodentes were in conical shape (75.0%). Sixty-seven percent of the cases were fully impacted.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Investigation of prevalence and characteristics of mesiodens in a non-syndromic 11256 dental outpatients.

AIM To investigate the prevalence of mesiodens in a sample of Turkish dental patients and their distribution among genders. PATIENTS AND METHODS A retrospective study was performed using panoramic radiography of 11256 patients, who ranged in age from 15 to 55 years old. All data (age, sex and or syndrome) were obtained from the patient files and analyzed for mesiodens. Statistical evaluation ...

متن کامل

Prevalence and characteristics of supernumerary teeth in a non-syndrome Turkish population: associated pathologies and proposed treatment.

OBJECTIVE The objectives of the present study were to investigate the prevalence and characteristics of supernumerary teeth and evaluate the associated pathologies and treatment protocol in a Turkish patient population. STUDY DESIGN A retrospective study was performed using full-mouth periapical and panoramic radiographs of 3491 patients (2146 females and 1345 males) ranging in age from 12 to...

متن کامل

Frequency of mesiodens in the pediatric population in North India: A radiographic study

OBJECTIVES Mesiodens are the most common supernumerary teeth, occurring in 0.15% to 2.2% of the population. The aim of the present study was to analyze the frequency and radiological features of mesiodens in the pediatric population. MATERIAL AND METHODS The study was based on the radiographic evaluation of 4133 pediatric patients of the age range of 4-15 years, attending the Department of Or...

متن کامل

Molecular Genetic Analysis of the Variable Number of Tandem-Repeat Alleles at the Phenylalanine Hydroxylase Gene in Iranian Azeri Turkish Population

Background: The variable numbers of tandem-repeat (VNTR) alleles at the phenylalanine hydroxylase (PAH) gene have been used in carrier detection and prenatal diagnosis in phenylketonuria families. This study was carried out to analyze VNTR alleles at the PAH gene in Iranian Azeri Turkish population. Methods: In this study, 200 alleles from general population were studied by PCR. Results: The fr...

متن کامل

High Frequency of IVS10nt546 Linked to VNTR8 in Iranian PKU Patients from Fars Province

Dear Editor Analysis of the phenylalanine hydroxylase (PAH McKusick 261600) gene in different populations has revealed more than 320 different mutations associated with phenylketonuria (PKU). One of these mutations, IVS10nt546, results in severe PAH deficiency due to defective mRNA splicing. It accounts for about 40 percent of all mutant alleles in Turkish and between 10 to 20 percent of all mu...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:

دوره 5  شماره 

صفحات  -

تاریخ انتشار 2011