Combined surgical-orthodontic rehabilitation of cleidocranial dysplasia: 5 years follow-up
نویسندگان
چکیده
منابع مشابه
Orthodontic and surgical management of cleidocranial dysplasia
Cleidocranial dysplasia (CCD), an autosomal dominant disorder with a prevalence of 1 in 1,000,000 individuals, is mainly caused by mutations in Runx2, a gene required for osteoblastic differentiation. It is generally characterized by hypoplastic clavicles, narrow thorax, and delayed or absent fontanel closure. Importantly, its orofacial manifestations, including midfacial hypoplasia, retained p...
متن کاملCleidocranial dysplasia
Cleidocranial dysplasia (CCD) is an autosomal dominant disorder resulting in the skeletal and dental abnormalities due to the disturbance in ossification of the bones. Clavicle is the most commonly affected bone. The prevalence of CCD is one in millions of live births. In this report, we present a case of 10-years-old boy showing features of this condition.
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Background: During last decades, many otologists attempted to make a long standing dry ear, resulting in better hearing after cholesteatoma surgery. This study evaluated the prognosis of two common methods of cholesteatoma ear surgery considering ten years follow-up. Methods: This retrospective analysis was done using medical records of 108 adult patients with cholesteatoma. After ten years of ...
متن کاملSurgery in Cholesteatoma: Ten years Follow-up
Dear Editor, I was greatly interested in the article "Surgery in cholesteatoma: Ten years Follow-up" by Dr. M. Ajalloueyan published in your journal in March 2006; Vol 31, No 1: 37-40.I think there are grave misconceptions and many doubts about this article. That article has some misleading data that should be clarified by the author. The descriptions of table 1, "Statistical characteristics of...
متن کاملFamilial Cleidocranial Dysplasia
Cleidocranial dysplasia or mutational dysostosis or cleidocranial dysostosis is a generalized skeletodental dysplastic disorder, inherited in an autosomal dominant pattern. The expression of this disorder can vary widely in severity, even within the same family. This is a relatively rare disease and has no standard effective treatment option as of yet. Here we present a case report of affected ...
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ژورنال
عنوان ژورنال: World Journal of Clinical Cases
سال: 2015
ISSN: 2307-8960
DOI: 10.12998/wjcc.v3.i8.751