dc.contributor.author | salah, Abdulraof | |
dc.date.accessioned | 2019-08-07T09:30:18Z | |
dc.date.available | 2019-08-07T09:30:18Z | |
dc.date.issued | 2018-06-27 | |
dc.identifier.uri | http://repository.limu.edu.ly/handle/123456789/1133 | |
dc.description | Cleidocranial dysplasia (CCD) is an uncommon but well-known genetic skeletal condition. Several
hundred affected persons are members of a large extended family The clinical manifestations are
often innocuous, but hyperdontia and other developmental abnormalities of the teeth are a major
feature and may require special dental management | en_US |
dc.description.abstract | Cleidocranial dysplasia is a condition that primarily affects development of the bones and teeth.
Signs and symptoms of cleidocranial dysplasia can vary widely in severity, even within the same
family.so this report will discuss the general, oral manifestation and pathogenesis. | en_US |
dc.language.iso | en | en_US |
dc.publisher | faculty of Basic Medical Science - Libyan International Medical University | en_US |
dc.rights | Attribution 3.0 United States | * |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/us/ | * |
dc.title | Clinical Manifestation and pathogenesis of Cleidocranial dysplasia | en_US |
dc.type | Other | en_US |