Detection and diagnosis of cleidocranial dysplasia by panoramic radiography
Y Shi, Z Ye, Y Liu, H Wang, M You - 2022 - researchsquare.com
Background The purpose of this study was to illustrate and quantify the maxillofacial bone
abnormalities detected on panoramic radiographs from a group of Chinese patients with …
abnormalities detected on panoramic radiographs from a group of Chinese patients with …
[PDF][PDF] UNIVERSIDAD NACIONAL AUTÓNOMA DE MÉXICO
MG HERNÁDEZ - ru.dgb.unam.mx
La dentición humana tiene características heterodontas y difiodontas. El primer término se
relaciona con la diversidad morfológica en la que se manifiesta la existencia de más de un …
relaciona con la diversidad morfológica en la que se manifiesta la existencia de más de un …
[引用][C] The importance of Dentistry in assisting individuals with birth defects
FD Santa Maria, BM de Oliveira, L Schuler-Faccini - 2021 - UFRGS
Case of odontoma-related infection in a cleidocranial dysplasia
A Martins, P Caixeirinho, A Fernandes - BMJ case reports, 2019 - search.proquest.com
Cleidocranial dysplasia (CCD) is a rare syndrome with an estimated prevalence of 1: 1 000
000.1 2 It has an autosomal dominant transmission with complete penetrance and variable …
000.1 2 It has an autosomal dominant transmission with complete penetrance and variable …
Estudios de imagen utilizados como ayuda en el diagnóstico de displasia cleidocraneal. Una revisión
LA Granado-Abasto… - Revista Científica …, 2021 - revistas.cientifica.edu.pe
La displasia cleidocraneal (DCC), también conocida como síndrome de Marie-Sainton, es
un trastorno poco común de tipo autosómico dominante, que presenta características …
un trastorno poco común de tipo autosómico dominante, que presenta características …
Marie-Sainton syndrome (cleidocranial dysplasia): early diagnosis is the key
Abstract Correspondence to Professor Neeta Mohanty; neetamohanty@ soa. ac. in
Description Marie-Sainton syndrome or cleidocranial dysplasia is a rare, autosomal …
Description Marie-Sainton syndrome or cleidocranial dysplasia is a rare, autosomal …
[PDF][PDF] A importância da Odontologia na assistência a indivíduos com defeitos congênitos
FD Santa Maria, BM de Oliveira… - Revista da Faculdade …, 2021 - researchgate.net
Introdução: Defeitos congênitos são alterações estruturais ou funcionais que acontecem
durante a vida intra-uterina. O cirurgião-dentista deve reconhecer os defeitos craniofaciais …
durante a vida intra-uterina. O cirurgião-dentista deve reconhecer os defeitos craniofaciais …
[PDF][PDF] IMAGING STUDIES USED AS AID IN THE DIAGNOSIS OF CLEIDOCRANIAL DYSPLASIA. A REVIEW
EDEIUC AYUDA - pdfs.semanticscholar.org
Cleidocranial dysplasia (CCD), also known as Marie-Sainton syndrome, is a rare disorder of
autosomal dominant type that presents specific characteristics at the skeletal and dental …
autosomal dominant type that presents specific characteristics at the skeletal and dental …
[PDF][PDF] Cleidocranial Dysostosis: Case report of a Jordanian family
N Nassrawin, A Heasat - siriusstore.com
Objectives: to describe Jordanian family three members of them diagnosed with
cleidocranial dysostosis and the treatment approaches for each one of them. Case …
cleidocranial dysostosis and the treatment approaches for each one of them. Case …
CLEIDOCRANIAL DYSPLASIA: A CASE REPORT
F Tahir, MH Piracha, F Hafeez, S Hassan… - Pakistan Journal of …, 2021 - pakjpath.com
Cleidocranial dysplasia (CCD) also known by the name of Marie and Sainton†s disease,
is a rare autosomal dominant disease characterized by multiple skeletal and dental …
is a rare autosomal dominant disease characterized by multiple skeletal and dental …