Occlusal morphology in Turner syndrome.

نویسندگان

  • M Midtbø
  • A Halse
چکیده

The prevalence of malocclusion in 32 Turner syndrome patients, age 7-16.7 years, was investigated. The sample was subdivided according to karyotype, and 72 normal girls, aged 7.1-16.1 years, served as controls. Compared with normal girls overjet did not differ significantly while overbite was significantly reduced in 45X patients. The prevalence of distal molar occlusion, anterior and lateral open bite and lateral crossbite was significantly increased. Most significant differences were found between 45X patients and controls. Mosaic and isochromosome for the long arm of X karyotypes showed the same pattern of malocclusion, but with greater variation. No significant differences were found comparing 45X patients with mosaic and isochromosome for the long arm of X karyotypes. The results indicate that patients with structural and/or numerical aberration of the X chromosome, develop a specific pattern of malocclusion with deviations in sagittal, vertical and transversal directions.

برای دانلود 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

Simultaneous Occurrence of Turner Syndrome and Robertsonian Translocation in a Girl with Short Stature: A Case Report

Short stature is an important clinical feature of Turner syndrome (TS). In this report, a girl with short stature suspected to have Turner syndrome underwent cytogenetic analysis, which confirmd Turner syndrome by observing sex chromosomal monosomy using the karyotype test. In addition to Turner syndrome, Robertsonian (ROB) translocation t(13;14) was detected. As recommended by a genetic counse...

متن کامل

Dextrocardia and Hiatal Hernia in a Patient with Turner Syndrome

Turner syndrome is a sex-chromosome disorder occurring in one out of 2500 female births and characterized by growth retardation, gonadal dysgenesis and cardiovascular anomalies. The 45, XO karyotype is the most frequent type of this disease. Herein, we report on a 6-year-old girl with Turner syndrome and 45, XO karyotype presenting with short stature. She had dextrocardia and hiatal hernia. To ...

متن کامل

Evaluation of the relationship between the back of the neck and the incidence of Turner syndrome in the first trimester of pregnancy

Abstract Background and Aim: Children with various anomalies are economically, emotionally charged for the family and society. The purpose of this study was to evaluate the value of Nuchal translucency (NT) in the diagnosis of Turner Syndrome in the first trimester of pregnancy. Materials and Methods: This prospective study was performed on 1522 pregnant women with gestational age of 11 to 13 w...

متن کامل

Comparison of classical cytogenetics versus interphase FISH in diagnosis of mosaic form of Turner syndrome

 Abstract  Background: Mosaic form of turner syndrome that represented by two or more  cell lines in an affected individual, often has limitation for detection with classical  cytogenetic methods. The present study was carried out to compare the efficiency of  interphase Fluorescence In Situ Hybridisation (FISH) and cytogenetic techniques in  detection of mosaic form of turner syndrome.  Method...

متن کامل

Effects of Karyotype Variations on Phenotype of Patients with Turner Syndrome

Background: Turner syndrome (TS) is a sporadic disorder caused by the absence of all or some parts one X-chromosome with major developmental consequences such as short stature and ovarian failure etc. The minor manifestations of TS are cubitus valgus, micrognatism, high-arched palate, short and/or webbed neck, hypothyroidism, etc. Different karyotype abnormalities may lead to different clinical...

متن کامل

Turner Syndrome: A Unique Mosaic Case with 45,X/47,XX,+21/46,XX Cell Lines

We report an extremely rare case of Turner syndrome mosaicism in a 30-year-old woman. At least 100 metaphases were observed and analyzed through GTG banding with over 550 band resolutions observed. G-banded chromosome analysis revealed a mosaic female karyotype involving 3 different cell lines. One cell line (90% of the analyzed metaphases) presented monosomy X, while 6% of the cells showed tri...

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

برای دانلود 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

عنوان ژورنال:
  • European journal of orthodontics

دوره 18 2  شماره 

صفحات  -

تاریخ انتشار 1996