Cleidocranial dysostosis: a report on two familial cases / Disostose cleidocraniana: relato de dois casos familiares
Radiol. bras
; Radiol. bras;46(6): 382-384, Nov-Dec/2013. graf
Article
in En
| LILACS
| ID: lil-699246
Responsible library:
BR1.1
ABSTRACT
Cleidocranial dysostosis is a rare genetic syndrome with an autosomal dominant inheritance pattern. The most common manifestations include clavicular aplasia or hypoplasia, open fontanelles and abnormal dentition. The present report describes two familial cases whose late diagnosis was made by means of clinical and radiographic findings. The treatment was radical, with complete surgical teeth extraction and making of total dental prosthesis.
Full text:
1
Collection:
01-internacional
Database:
LILACS
Language:
En
Journal:
Radiol. bras
Journal subject:
DIAGNOSTICO POR IMAGEM
/
RADIOLOGIA
Year:
2013
Document type:
Article
Affiliation country:
Brazil
Country of publication:
Brazil