نتایج جستجو برای: dental anomaly

تعداد نتایج: 199327  

2016
Marco Antonio García Castillo Silvia Tavira Fernández

In human dentition characteristics, complex processes intervene that have a close relationship with the growth and development of the whole craniofacial complex mainly in bones such as the maxilla and the mandible. Dental morphology is determined by environmental and genetic factors which are in a dynamic relationship that may cause single, partial or complete anomalies in dental development. D...

2015
Elena Di Palma Biagio Di Giuseppe Michele Tepedino Claudio Chimenti

INTRODUCTION Maxillary canine-first premolar transposition (Mx.C.P1) is an uncommon dental positional anomaly that may create many orthodontic problems from both esthetic and functional points of view. OBJECTIVE In this report we show the orthodontic management of a case of Mx.C.P1 associated with bilateral maxillary lateral incisor agenesis and unilateral mandibular second premolar agenesis ...

2017
Karen de Almeida Pinto Fernandes Karina de Almeida Pinto Fernandes Thiago Jeunon de Sousa Vargas Daniel Fernandes Melo

Woolly hair nevus is a rare condition characterized by a structural anomaly of the hair, restricted to certain areas of the scalp. The hair becomes coiled and slightly hypopigmented. The term woolly hair refers to changes that affect all the scalp and has a hereditary character. We present a case of woolly hair nevus, that developed at the age of 2 years, associated with dental diastema and ver...

The Ellis-van Creveld (EVC) syndrome is a chondroectodermal dysplasia and is characterized by the cardinal features of disproportionate short stature, polydactyly, hidrotic ectodermal dysplasia, and congenital heart malformations, along with other skeletal and dental abnormalities. It is a rare condition, with very few cases reported in the medical literature. It is inherited as an autosomal re...

Journal: :Chang Gung medical journal 2011
Ting-Ting Wu Philip K T Chen Lun-Jou Lo Min-Chi Cheng Ellen Wen-Ching Ko

BACKGROUND Dental anomalies associated with different severities of cleft lip and palate have been rarely reported. This retrospective study investigates the characteristics of dental anomalies associated with different types of cleft, and compares the dental anomaly traits based on sex and severity of cleft. METHODS Cleft patients born in 1995 with qualified diagnostic records from 7 to 11 y...

2007
Kenneth D. Rose Holly Smith Frank Carpenter KENNETH D. ROSE

2014
Nikhil Grover

Regional odontodysplasia (RO) is a sporadic (not inherited) developmental defect involving only a few contiguous teeth in a small region of the jaw; developmentally it involves both mesodermal and ectodermal dental components. It affects the primary and permanent dentition in the maxilla and mandible or both jaws. Generally it is localized to only one arch. The etiology of this dental anomaly i...

2013
Suresh Yadav Shallu Tyagi Prince Kumar Divya Sharma

Fusion of teeth is the union of two or more tooth germs, which are usually separated. Depending upon the stage of odontogenesis, it can be complete or incomplete. The present case describes fusion between the maxillary primary right central and lateral incisor with a supernumerary tooth. Clinical and radiographic examination revealed the presence of fused triple teeth. The fused teeth were extr...

Journal: :Approaches in poultry, dairy & veterinary sciences 2022

Approaches in Poultry, Dairy & Veterinary Sciences The First Confirmed Case of Dental-Skeletal- Retinal-Anomaly (DSRA) the Cane Corso Italiano Dog Breed Czech Republic Korec E*, Elblová P and Králová J Department Genetics, ZOO Tábor, *Corresponding author: Evžen Korec, Submission: January 13, 2022;Published: 24, 2022 DOI: 10.31031/APDV.2022.08.000699 ISSN: 2576-9162 Volume8 Issue5

Journal: :thrita 0
zohreh kavehmanesh department of pediatrics, faculty of medicine, baqiyatallah university of medical sciences, tehran, iran ali reza shafiee student research committee, baqiyatallah university of medical sciences, tehran, ir iran; student research committee, baqiyatallah hospital, molasadra street, vanak place, tehran, ir iran. tel: +98-9192525889, fax: +98-2181264354

introduction robinow syndrome (rs) is an infrequent genetic condition that is characterized by a dysmorphic face, dental anomaly, short stature, mesomelic limb shortening, hand and foot anomalies, and hypoplastic genitalia. the robinow syndrome has been reported from the arab countries and other asian countries, but has not been reported in iranian population so far. case presentation a new bor...

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