Results 31 to 40 of about 119,862 (124)
Detection of bifid mandibular condyle by panoramic radiography and cone beam computed tomography [PDF]
Aim: To compare panoramic radiography and cone beam computed tomography (CBCT) in the diagnosis of bifid mandibular condyle. Methods: The sample consisted of 350 individuals who underwent panoramic radiography and CBCT.
de Freitas, Deborah Queiroz +5 more
core +1 more source
Bifid mandibular condyle: A rare disorder
Bifid mandibular condyle is a rare disorder and little is known about the etiology and pathogenesis. We reported a patient with left bifid mandibular condyle with a history of trauma.
Mavili, M. Emin +2 more
core +1 more source
Bifid mandibular condyle (BMC) is a rare asymptomatic morphological alteration with no predilection for age group or gender. Its morphology varies from a shallow groove to two condylar heads with separate necks, oriented mediolaterally or ...
Melo, DP +5 more
core +1 more source
Aim: The aim of this study was to determine the prevalence and gender predilection of bifid mandibular condyle (BMC) in Indian population using extra oral radiographs.
Bhawandeep Kaur, Sarfaraz Padda
doaj +1 more source
We evaluated the anatomical variations of the mandibular canal associated with various facial types, age, sex, and side of the face studied. We analyzed 348 hemimandibles in subjects without a history of trauma, lesions in the lower arch, or orthognathic or repair surgery in the posterior mandible. Facial type was determined using the VERT index.
Rudyard dos Santos Oliveira +4 more
wiley +1 more source
Background. The retromolar canal (RMC) is an anatomical variation that can cause complications in dental procedures. Method. The RMC was evaluated according to age, sex, and presence of accessory mandibular canal and accessory mental foramen, on both sides in 500 panoramic radiographs, belonging to individuals at the age of 7 to 20 years.
Ticiana Sidorenko de O. Capote +3 more
wiley +1 more source
Abstract Trichorhinophalangeal syndrome (TRPS) is a rare genetic disease inherited in an autosomal dominant manner. It occurs in 1 in 100,000 people globally and is caused by several types of mutations of the TRPS1 gene. Since the first human patient was reported in 1966, typical and atypical pathologies, disease courses, and treatment case ...
Naoya Saeki +6 more
wiley +1 more source
Binary Logistic Regression Analysis of Foramen Magnum Dimensions for Sex Determination
Purpose. The structural integrity of foramen magnum is usually preserved in fire accidents and explosions due to its resistant nature and secluded anatomical position and this study attempts to determine its sexing potential. Methods. The sagittal and transverse diameters and area of foramen magnum of seventy‐two skulls (41 male and 31 female) from ...
Venkatesh Gokuldas Kamath +4 more
wiley +1 more source
Objective. To evaluate the efficiency of DVT in comparison with OPG in the assessment of bony condylar changes in patients of TMJ pain. Methods. 100 temporomandibular joints of 62 patients with the complaint of temporomandibular joint pain were included in the study. DVT and OPG radiographs were taken for all the 100 joints. Three observers interpreted
Ujwala Shivarama Shetty +4 more
wiley +1 more source
Condylar Aplasia and Hypoplasia: A Rare Case
Aplasia of condyle is very rare, when this condition not seen as a part of a syndrome. We report a case of condylar aplasia on the right side and hypoplasia on the left side in a 21‐year‐old female. The patient reported to the department with a chief complaint of underdeveloped lower jaw.
Peeyush Shivhare +6 more
wiley +1 more source

