Results 51 to 60 of about 1,866 (155)
Taurodontism: from Neanderthals till modern human population [PDF]
, 2016 Introduction. Taurodontism is an aberration of teeth that lacks the constriction at the level of the CEJ and characterized by elongated pulp chambers and apical displacement of bifurcation or trifurcation of the roots, giving it a rectangular shape. Aim.
Tineshev, Slavi, Tomov, Georgi
core
Endodontic Treatment of a Taurodontism Tooth: Report of a Case
, 2008 Taurodontism is a rare dental anomaly in which the involved tooth has an enlarged and elongated body and pulp chamber with apical displacement of the pulpal floor.
MirMotalebi, Farshid, Nazari, Shahrzad
core +1 more source
Prevalence of dental anomalies on panoramic radiographs in a population of the state of Pará, Brazil
Indian Journal of Dental Research, 2014 Introduction: Dental anomalies (DAs) are the result of disorders that are able to modify the shape, number, size, and structure of teeth. This study aimed to evaluate the prevalence of DAs using panoramic radiographs in a population of the City of Belém,
Antonio JG Goncalves.Filho +5 more
doaj +1 more source
Clinical Case Reports, Volume 14, Issue 5, May 2026.ABSTRACT Dens invaginatus (DI) is a developmental anomaly characterized by the invagination of enamel and dentin into the pulp space, predisposing affected teeth to pulpal and periapical pathologies. The complex and irregular canal anatomy often complicates endodontic management.
Chloé Laporte +2 more
wiley +1 more source
مجله دانشکده دندانپزشکی اصفهان, 2013 Introduction: Few studies have assessed the prevalence of taurodontism in Iranian populations. The aim of this descriptive study was to investigate the frequency of taurodont teeth among dental patients attending two radiology centers in Tehran, Iran ...
Vahid Rakhshan +2 more
doaj
Ellis-van Creveld syndrome with unusual oral and dental findings: A rare clinical entity
Dental Research Journal, 2016 Ellis-van Creveld (EVC) syndrome, a form of skeletal and chondroectodermal dysplasia, is an autosomal recessive disorder characterized by a tetrad of disproportionate dwarfism, postaxial polydactyly, ectodermal dysplasia, and heart defects.
Sameeulla Shaik +3 more
doaj +1 more source
Saudi Journal of Oral Sciences, 2021 Genetic disorders of the dentin are known for several years, and reviews have been published mainly in the form of case reports. Dentinogenesis imperfecta (DI) is a disease characterized by an abnormal formation and abnormal structure of the dentin ...
Vela D Desai, Rajeev Chitguppi
doaj +1 more source
American Journal of Medical Genetics Part A, Volume 200, Issue 4, Page 790-799, April 2026.ABSTRACT TSPEAR (chr. 21q22.3) encodes a protein involved in tooth development and is predominantly expressed in the enamel knot. Biallelic loss of function variants in TSPEAR cause ectodermal dysplasia, tooth agenesis and sensorineural hearing loss. However, the role of TSPEAR in auditory processes is unclear.
Debora Vergani +17 more
wiley +1 more source
Tooth Agenesis and Associated Tooth Developmental Anomalies
Česká Stomatologie a Praktické Zubní Lékařství, 2014 Aim of study: Tooth agenesis means absence or incomplete development of tooth. It is the most common developmental dental anomaly in man. The prevalence of agenesis in permanent dentition (excluding third molars) in common population oscillates between 2.
L. Kramerová +3 more
doaj +1 more source
Nance‐Horan Syndrome: Further Delineation of the Affected Male and the Female Carrier Phenotypes
American Journal of Medical Genetics Part A, Volume 200, Issue 3, Page 642-652, March 2026.ABSTRACT Nance‐Horan syndrome (NHS; OMIM 302350) is a rare, X‐linked syndrome characterized by bilateral congenital cataracts leading to profound vision loss, specific dental anomalies including characteristic screwdriver blade‐shaped incisors, facial anomalies, and intellectual disability.
Maria K. Haanpää +14 more
wiley +1 more source