Results 51 to 60 of about 2,507 (167)

Clidocraneal dysostosis: Literature review and report of a clinical case.

open access: yes, 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
core   +1 more source

Cleidocranial dysostosis: report of a case

open access: yes, 1997
This case of cleidocranial dysostosis showed nearly 40 accessory teeth and the unerupted teeth on radiological examinations. Other diagnostic procedures found hypoplasia in maxillary and zygomatic bones, deep palate, open fontanel and open sutures, the ...

core  

Yunis Varon Syndrome [PDF]

open access: yes, 2010
We have reported a case of Yunis-Varon syndrome which is a rare, autosomal recessive syndrome characterized by growth retardation, defective growth of the cranial bones, characteristic facial features, abnormalities of the fingers and/or toes ...
Parmar, P   +3 more
core  

Cleidocranial dysostosis: case report

open access: yes, 2017
Cleidocranial dysostosis (CCD) is a rare congenital bone disorder with an autosomal dominant genetic pattern, which has a prevalence of 1 in 1 million. It is caused mainly by a mutation in the RUNX2 transmission gene, a gene required for differentiation ...
Marcon, Tayane Vicenço
core  

Cone beam computed tomography and prosthodontic rehabilitation of cleidocranial dysostosis

open access: yes, 2013
The aim of this study is to present a clinical case of a male patient with cleiodocranial dysostosis, in which the cone beam tomography was crucial in the decision making regarding the type of prosthetic rehabilitation to ...
Inês Côrte-Real   +4 more
core   +1 more source

Nonfamilial cleidocranial dysplasia (dysostosis): a case report

open access: yes, 1990
Consultant, Dental Department, King Fahd Central Hospital,P.O.Box 204, Gizan, Saudi ArabiaCleidocranial dysplasia, previously known as cleidocranial dysostosis, is a rare hereditary disease of unknown etiology characterized by abnormalities in the skull,
Salem, G.
core  

Interim Prosthetic Phase of Multidisciplinary Management of Cleidocranial Dysplasia: “The Bronx Approach”

open access: yes, 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
core   +1 more source

Sequential supernumerary teeth development in a non-syndromic patient; report of a rare case.

open access: yesFrontiers in Dentistry, 2013
Isolated impacted supernumerary teeth are quite rare, but they can be seen associated with several syndromes such as cleidocranial dysostosis or Gardner's syndrome.
Mohammad Jafarian   +4 more
doaj  

Disostosis cleidocraneal. Estudio familiar

open access: yesRevista Cubana de Medicina, 2002
Se estudió la disostosis cleidocraneal, enfermedad hereditaria del esqueleto que se transmite en forma autosómica dominante. Se analizaron 4 sujetos correspondientes a 3 generaciones de una misma familia.
Rafael Arocha Rodríguez   +3 more
doaj  

Cleidocranial dysplasia - A case report

open access: yes, 2011
Cleidocranial dysplasia (Dysostosis) is an autosomal dominant disease with a wide range of expression, characterized by clavicular aplasia or hypoplasia, defective ossification, retarded cranial ossification, delayed bone and teeth development ...
Uday Y Shankar
core  

Home - About - Disclaimer - Privacy