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CHARGE syndrome: Genetic aspects and dental challenges, a review and case presentation
(Springer Nature, 2020)
CHARGE syndrome (CS) is a rare genetic condition (OMIM #214800). The condition has a variable
phenotypic expression. Historically, the diagnosis of CHARGE syndrome was based on the presence of specific
clinical criteria. ...
The evolution of the nosology of osteogenesis imperfecta
(Wiley-Blackwell, 2021)
Osteogenesis imperfecta (OI) is a relatively common genetic skeletal disorder with an estimated frequency of 1 in 20 000 worldwide. The manifestations are diverse and although individually rare, the several different forms ...
Sella turcica morphology in patients with genetic syndromes: Protocol for a systematic review
(JMIR Publications Inc., 2020)
Background: The sella turcica is an important anatomical reference used in orthodontics and the evaluation of craniofacial growth. Studies have found an association between variations in sella turcica morphology in patients ...
Taurodontism in dental genetics
(Springer Nature, 2021)
Taurodontism is a dental anomaly defined by enlargement of the pulp chamber of multirooted teeth with apical displacement of
the pulp floor and bifurcation of the roots. Taurodontism can be an isolated trait or part of a ...