Results 101 to 110 of about 3,948 (205)
Cleidocranial Dysplasia: A Case Report
Journal of Clinical Research in Pediatric Endocrinology, 2010 Cleidocranial dysplasia (CCD) is a rare autosomal dominant skeletal disease. CCD is caused by mutation in the gene on 6p21 encoding transcription factor CBFA1, i.e. runt-related transcription factor 2(RUNX2). The disease is characterized by a persistently open anterior fontanelle and skull sutures, hypoplastic or aplastic clavicles, dental ...
Karagüzel, Gülay +5 more
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Orthodontic Care of Cleidocranial Dysplasia Patients
Turkish Journal of Orthodontics, 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
doaj +1 more source
Multiple Supernumerary Teeth in a Non-Syndromic Patient: A Case Report [PDF]
, 2013 Introduction: Multiple supernumerary teeth are a rare phenomenon. It occurs more often in patients with syndromes such as Gardner's syndrome, cleidocranial dysplasia and so on. This phenomenon in absence of such syndromes is rare.
Baratollah Shaban +2 more
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Journal of Education, Health and Sport, 2016 Szczepkowska Aleksandra, Osica Piotr, Janas-Naze Anna. Aspekt chirurgiczny opieki nad pacjentem z dysplazją obojczykowo-czaszkową – opis przypadku = Surgical aspect of patient care with cleidocranial dysplasia - case report.
Aleksandra Szczepkowska +2 more
doaj +2 more sources
A multi-centre evaluation of multiple supernumerary premolar prevalence
Australasian Orthodontic Journal, 2015 The occurrence of multiple supernumerary teeth is rare and often found in association with syndromes such as cleidocranial dysplasia, Gardner's syndrome or cleft lip and palate.
Gunduz Kaan +6 more
doaj +1 more source
Cleidocranial dysplasia: A case report
Journal of Indian Society of Pedodontics and Preventive Dentistry, 2008 Cleidocranial dysplasias is an autosomal dominant disorder that presents with skeletal dysplasia. The dental manifestations are mainly delayed exfoliation of primary teeth and delayed eruption of permanent teeth, with multiple impacted supernumeraries ...
Hemalatha R, Balasubramaniam M
doaj
Cleidocranial dysplasia: a case report
مجله دانشکده دندانپزشکی اصفهان, 2009 Introdution: Cleido cranial Dysplasia (CCD) is a rare autosomal dominant disorder affecting skull and clavicle and may be accompanied by some other skeletal abnormalities.
P Ghalyani, N Sarrafan
doaj
Manifestation and treatment in a cleidocranial dysplasia patient with a RUNX2 (T420I) mutation [PDF]
, 2015 core +1 more source
Poliposis familiar hereditaria y síndrome de Gardner: aportación de la exploración odontoestomatológica a su diagnóstico y descripción de un caso [PDF]
, 2005 La poliposis adenomatosa familiar (PAF) y su variante fenotípica, el síndrome de Gardner, constituyen una infrecuente patología hereditaria autosómica dominante.
Blanco, Ignacio +3 more
core +1 more source
Turkiye Klinikleri Journal of Dental Sciences, 2021 Fatma Nur YOZGAT İLBAŞ +1 more
openaire +1 more source