نتایج جستجو برای: hypodontia
تعداد نتایج: 614 فیلتر نتایج به سال:
Agenesis of bilateral maxillary canines is very rare and mesiodens is a commonly occurring supernumerary tooth type. Concomitant occurrence of both hypodontia and hyperdontia is extremely rare and it is a condition of mixed numeric variation in the same individual. The reported prevalence of this condition ranges between 0.002% and 3.1%. The purpose of this case report is to describe a rare occ...
A case of Kabuki syndrome in a ten-year old male is presented with a review of published literature. This rare autosomal dominant condition presents with a number of characteristic dermatoglyphic abnormalities and facial features and other associated developmental anomalies and oral findings. The presence of hypodontia and other dental morphological abnormalities, such as root and crown anomali...
Background and Aim: Ectodermal dysplasia (ED) is a hereditary disease that affects ectodermal tissues. Its oral manifestations include hypodontia or oligodontia, which cause the reduction of the height and width of the alveolar ridge. Considering numerous difficulties that these patients encounter with regard to facial appearance, talking, and chewing, their rehabilitation has a major influence...
Rajendrasinh Rathore1, Rashmi GS Phulari2, Shivani Jain3 1Professor, Department of Oral and Maxillofacial Pathology and Microbiology, Manubhai Patel Dental College and Oral Research Institute, Vadodara, Gujarat, India, 2Reader, Department of Oral and Maxillofacial Pathology and Microbiology, Manubhai Patel Dental College and Oral Research Institute, Vadodara, Gujarat, India, 3Post-graduate Stud...
Russell-Silver syndrome (RSS) is a congenital disease characterized by short stature due to growth hormone deficiency, physical asymmetry, inverted triangular face, micrognathia, prominent forehead, and hypodontia. This case report presents a prosthetic management of a 6-year-old patient with Russell-Silver syndrome treated with overdentures on the maxilla and the mandible using the remaining p...
Ellis-van Creveld syndrome is a genetic disorder that was first described by Richard Ellis and Simon van Creveld in 1940. The four principal characteristics are chondrodysplasia, polydactyly, ectodermal dysplasia and congenital heart defects. The orofacial manifestations include multiple gingivolabial musculofibrous fraenula, dental anomalies, hypodontia and malocclusion. The disease can be dia...
Materials & Method: Study models of 464 orthodontic patients (165 male and 299 female) of the age ranging from 11 to 30 years were studied to evaluate the prevalence of malocclusion using Angle’s classification and occlusal characteristics of overjet, overbite, open bite, cross bite, displacement, and hypodontia according to the method of Dental Health Component of Index of Orthodontic Treatmen...
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