Results 41 to 50 of about 23,183 (161)
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
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
A new phenotype of EVEN-PLUS syndrome in a Chinese family and literature review. [PDF]
HSPA9 gene mutations should be suspected in all cases with specific craniofacial features, abnormal skeletal presentations, congenital heart defects, and renal alterations. Seizures and basal ganglia lesions are a new phenotype of Epiphyseal, Vertebral, Ear, and Nose‐PLUS syndrome.
Liu M, Li H, Ren S, Ding C.
europepmc +2 more sources
Excavation at University College London revealed more than 8700 human skeletal fragments representing at least 38 individuals, alongside over 800 animal remains. Features consistent with dissection, specimen preparation and curation provide evidence for the use of human and animal material in nineteenth‐century anatomical education, offering rare ...
Wendy Birch, Tania Kausmally
wiley +1 more source
Abstract Freshwater fishes from the northwestern Colombian Andes are reported from the Pliocene Sincelejo and Ware formations. A total of 10 taxa have been identified, involving two orders, five families and nine genera. Characters from dental morphology, fin spines and cranial bones are provided as taxonomic tools for the study of fossil fishes.
Gustavo A. Ballen +6 more
wiley +1 more source
Evaluation of bifid mandibular condyle prevalence Southeastern Anatolia of population by using cone beam computed tomography: A retrospective study [PDF]
Amaç: Bifid mandibular kondil (BMK) diğer ismiyle çift başlı kondil, mandibular kondil başının ikizleşmesi ile karakterize nadir gö rülen bir durumdur. BMK etiyolojisi tam olarak bilinmemekle beraber gelişimsel ya da travma sonucu oluşabilmektedir.
Güler, Rıdvan +3 more
core +1 more source
Abstract Dysalotosaurus lettowvorbecki (Ornithopoda, Dinosauria) is a small‐sized dryosaurid iguanodontian known from various isolated remains collected from the Tendaguru Formation (Upper Jurassic, Tanzania). Micro‐computed tomography of a small individual encased in a block offered a unique opportunity to describe c.
Riccardo Rocchi +3 more
wiley +1 more source
Goldenhar syndrome is a syndrome of complex structures developing from first and second branchial arches during blastogenesis. The etiology of this rare disease is not fully understood, as it has shown itself variable genetically and of unclear causes ...
Neeraj Sharma, Sidhi Passi
doaj +1 more source
An overview of the postcranial osteology of caecilians (Gymnophiona, Lissamphibia)
Abstract Caecilians comprise a relatively small (~220 species) group (Gymnophiona) of snake‐like or worm‐like, mostly tropical amphibians. Most adult caecilians are fossorial, although some species may live in aquatic or semi‐aquatic environments, either as larvae or adults.
Rodolfo Otávio Santos +2 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

