Results 131 to 140 of about 11,727 (288)
A novel PAX9 mutation found in a Chinese patient with hypodontia via whole exome sequencing.
Oral Diseases, 2018 OBJECTIVE To investigate a novel gene mutation in a Chinese patient with non-syndromic hypodontia. SUBJECTS AND METHODS Mutation analysis was carried out by whole exome sequencing.
Tingting Zhang +6 more
semanticscholar +1 more source
Prevalence and pattern of hypodontia in the permanent dentition of 3374 Iranian orthodontic patients
Dental Research Journal, 2012 Background : Hypodontia is the most common dental anomaly and might cause clinical complications. The aim of this study was to assess the prevalence and pattern of congenital missing in the permanent dentition dentition (excluding third molars), among ...
Fariborz Amini +2 more
doaj +1 more source
Hypodontia and hypoplasia of mandible: A rare defect caused by combination therapy
Journal of Pharmacy and Bioallied Sciences, 2013 Hypodontia is defined as the developmental absence of one or more tooth and it can present in varying degrees of severity and severe hypodontia has been defined as the absence of six teeth, excluding third molars. Radiation plays an important role in the
Senthil Kumar, Nazargi Mahabob
doaj +1 more source
Unknown syndrome: congenital heart disease, ptosis, hypodontia, and craniosynostosis. [PDF]
, 1989 Lakshmi Mehta, I J Lewis, M A Patton
openalex +1 more source
Valutazione delle anomalie dentarie in soggetti con differenti tipi di schisi orofacciali [PDF]
, 2017 Background and aim: Subjects with nonsyndromic cleft lip and/or palate (CLP) present high frequency of hypodontia, both inside and outside the cleft region, which may represent a complicating factor for the dental management.
Uomo, Roberto
core +1 more source
Hypodontia of permanent teeth among Middle Palaeolithic hominids: an early case dated to ca. 92 000±5000 years BP at the Qafzeh site [PDF]
, 1998 Anne-Marie Tillier +3 more
openalex +1 more source
Meðferð sjúklings með meðfædda tannvöntun [PDF]
, 2008 Neðst á síðunni er hægt að nálgast greinina í heild sinni með því að smella á hlekkinn View/OpenInngangur Meðfædd tannvöntun færri en sex fullorðinstanna að undanskildum endajöxlum (hypodontia) er álitin vera til staðar hjá um það bil 7-8% fólks samkvæmt
Ellen Flosadóttir,
core
Journal of Dental Sciences, 2011 Background/purpose: The aims of this study were to determine the frequency and distribution of developmental anomalies in the permanent teeth of a Turkish orthodontic patient population and determine the relationships between gender and dental anomalies.
Fatih Kazanci +4 more
doaj +1 more source
Интердисциплинарен пристап и план на терапија кај пациенти со олигодонција [PDF]
, 2018 Oligodontia is a rare developmental dental anomaly in humans characterized by the absence of six or more teeth. In European populations the estimated prevalence of both syndromic and non- syndromic oligodontia is 0.14%.
Dzipunova, Biljana +7 more
core +1 more source