Results 41 to 50 of about 2,661 (168)
Case Reports in Dentistry, Volume 2025, Issue 1, 2025.Introduction: Gemination and fusion are rare developmental anomalies that can present significant diagnostic challenges. Due to the complexity of distinguishing between these conditions, the term “double tooth” is commonly employed in clinical practice.
Matteo Pellegrini +6 more
wiley +1 more source
Multiple supernumerary teeth and possible implications
, 1987 A case of an unusual number of supernumerary teeth is reported because patients who present with this symptom may be suffering from Gardner's syndrome or cleidocranial dysostosis.
Acton, Caroline H. C.
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Cementum analysis in cleidocranial dysostosis
Indian Journal of Dental Research, 2008 Objective: Cleidocranial dysostosis (CCD) is a skeletal disorder associated with dental anomalies such as failure or delayed eruption of permanent teeth and multiple impacted supernumerary or permanent teeth.
Manjunath K +4 more
doaj
Updated EUROCAT guidelines for classification of cases with congenital anomalies
Birth Defects Research, Volume 116, Issue 2, February 2024.Abstract Background Precise and correct classification of congenital anomalies is important in epidemiological studies, not only to classify according to etiology but also to group similar congenital anomalies together, to create homogeneous subgroups for surveillance and research.
Jorieke E. H. Bergman +7 more
wiley +1 more source
An insight into the malocclusion of cleidocranial dysplasia [PDF]
, 2012 Cleidocranial dysplasia (CCD), formerly known as Cleidocranial dysostosis,is a rare congenital disorder of bone that is characterised by aplasia of, or deficient, clavicular formation, delayed and imperfect ossification of the cranium, relatively short ...
Dawjee, Salahuddien M. +2 more
core
Clidocraneal dysostosis: Literature review and report of a clinical case.
, 2012 Cleidocranial dysostosis (CCD) is a rare congenital skeletal disorder associated to clavicular hypoplasia or aplasia, delayed closure of fontanelles head with brachycephalic type, delayed exfoliation of primary teeth, delayed eruption of permanent teeth,
Bernardita Toro +2 more
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Orthodontic Care of Cleidocranial Dysplasia Patients [PDF]
, 2015 Cleidocranial dysplasia (CCD) is a rare congenital deformity inherited as an autosomal genetic trait with the prevalence of 1:1,000,000. It is characterized by dental defomities such as retained primary teeth, presence of supernumerary teeth, skeletal ...
Rahime Burcu Nur +2 more
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, 2011 This case report presents treatment of two patients with the usual characteristics of Cleidocranial Dysostosis. A multidisciplinary approach using the disciplines of prosthodontics, orthodontics, and oral surgery was effected.
Robert W. Berg +7 more
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The p38 MAPK pathway is essential for skeletogenesis and bone homeostasis in mice [PDF]
, 2010 Nearly every extracellular ligand that has been found to play a role in regulating bone biology acts, at least in part, through MAPK pathways. Nevertheless, much remains to be learned about the contribution of MAPKs to osteoblast biology in vivo. Here we
Zhai, Bo +33 more
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Multiple unerupted and supernumerary teeth in a patient with cleidocranial dysplasia [PDF]
, 2018 Cleidocranial dysplasia is an extremely rare familial disorder characterized by partial or complete absence of clavicles, characteristic craniofacial deformities, and the presence of numerous supernumerary and unerupted teeth.
Galal Omami, BDS, MSc, MDentSc, FRCD(C)
core +2 more sources