regional odonto dysplasia: a case report

نویسندگان

مجید برگ ریزان

majid bargrizan dental school, shahid beheshti university of medical sciences, tehran- iran.دانشکده دندانپزشکی، دانشگاه علوم پزشکی شهید بهشتی مهدی رنجپور

mahdi ranjpour dental school, shahid beheshti university of medical sciences, tehran- iran.دانشکده دندانپزشکی، دانشگاه علوم پزشکی شهید بهشتی بهنام اسلامی

behnam eslami dental school, shahid beheshti university of medical sciences, tehran- iran.دانشکده دندانپزشکی، دانشگاه علوم پزشکی شهید بهشتی فاطمه مشهدی عباس

fateme mashhadi abbas dental school, shahid beheshti university of medical sciences, tehran- iran.دانشکده دندانپزشکی، دانشگاه علوم پزشکی شهید بهشتی

چکیده

background & aim: regional odonto dysplasia (rod) is an unusual nonhereditary of teeth with significantly clinical and radiographic features. affected teeth usually remain unerupted or semi-erupted with a discolaration and irregular shape. radiographically these teeth have a large pulp chamber and thin layer of enamel and dentin with similar density. this article is introducing a female patient who was affected by regional odonto dysplasia (rod) (a developmental abnormality) and treatment of this patient. case report: this patient is a ten-year-old girl was referred to us with unerupted anterior maxillary teeth. her parents stated that the cba a teeth were extracted at the age of 3 for infection. at the first appointment the erupted left maxillary central tooth had malformation, discoloration and a related fistula with infected drainage. the 321 teeth germs were not erupted. due to surgical procedure the left permanent incisor ( 1 ) was extracted and right permanent central, lateral and canine ( 321 ) were enucleated, and appropriate prosthetic treatment was performed for patient after a while.j dent sch 2004 22(2): 203

برای دانلود باید عضویت طلایی داشته باشید

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

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Dentin Dysplasia: ARare Case Report

Introduction: Dentin Dysplasia is one of the rare hereditary diseases that the enamel is normal, but it also affects the dentin and  the shape of the tooth pulp. Due to the low prevalence of this disease, a case of dentin dysplasia with the classical and atypical dentin dysplasia type 1 is presented. Case presentation:A 11-year-old girl with the mobility of lower central teeth that has severe ...

متن کامل

Familial Cleidocranial Dysplasia in a Neonate: A Case Report

Background: Cleidocranial dysplasia (CCD) is a rare inherited skeletal dysplasia, with an incidence of 1 case per 1000,000 individuals. It is a form of predominantly autosomal dominant inheritance and is associated with a mutation in runt related transcription factor-2 gene mapped on chromosome 6p21. This disease primarily affects the bones formed by intramembranous ossification and is characte...

متن کامل

Thanatophoric Dysplasia; a Rare Case Report on a Congenital Anomaly

The rare form of skeletal dysplasia is thanatophoric dysplasia. The meaning for thanatophoric dysplasia is death bearing which is derived from Greek word. It occurs 1in 20,000 to 50,000. It is mainly due to mutations in the fibroblast growth factor receptor 3gene. Features of thanatophoric dysplasia are frontal bossing, prominent eyes, narrow thorax, protruded abdomen and bowed legs. The knowle...

متن کامل

Placental Mesenchymal Dysplasia With Normal Fetus: A Rare Case Report

Placental mesenchymal dysplasia (PMD) is a rare benign placental abnormality. It is characterized by hydropic degeneration of stem villi, placentomegaly, and increased maternal serum alpha-fetoprotein(AFP). It can be associated with different congenital abnormalities, karyotype abnormalities, and feto-maternal morbidities. It is difficult to differentiate PMDfrom partial mole, complete mole wit...

متن کامل

Chondroectodermal dysplasia (Ellis-Van Creveld syndrome: A case report

Ellis-Van Creveld syndrome is a very rare congenital disorder which its principal features are polysyndactyly, chondrodysplasia, cardiac abnormalities and ectodermal dysplasia. We report a 10-year-old girl with major manifestations of this syndrome who also had multiple brownish macules and patches on trunk and extremities with aortic and pulmonary stenosis in echocardiographic evaluations.

متن کامل

Bone Fibrosis Dysplasia - Gastrointestinal Case Report

Un cas de fihreuse dysplasie evoluant dcpuis dix ans a ete observe a l'hopital farahnaz de l'universite Melli de Teheran. La particu-larite in terssante de cettc patiente est tout d'abord la clegenerscence kystiquc de foyer de l'os iliaque droit et la multitude des fractures des membres ayant consolide dans des positions v1cieusc spon tanement. Presence d'un foyer temporal gauchf! de .forme scl...

متن کامل

منابع من

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


عنوان ژورنال:
journal of dental school, shahid beheshti university of medical sciences

جلد ۲۲، شماره ۲، صفحات ۲۰۳-۲۱۱

کلمات کلیدی

میزبانی شده توسط پلتفرم ابری doprax.com

copyright © 2015-2023