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| Content Provider | World Health Organization (WHO)-Global Index Medicus |
|---|---|
| Author | Bandlapalli, Anila Singhal, Parul Singhal, Anita Jayam, Cheranjeevi |
| Description | Author Affiliation: Singhal P ( Department of Paediatric Dentistry, Himachal Pradesh Government Dental College, Shimla, Himachal Pradesh, India.); Singhal A ( Himachal Pradesh Government Dental College, Shimla, Himachal Pradesh, India.); Jayam C ( Department of Paediatric Dentistry, Himachal Pradesh Government Dental College, Shimla, Himachal Pradesh, India.); Bandlapalli A ( Department of Conservative Dentistry and Endodontics, Himachal Dental College, Shimla, Himachal Pradesh, India.) |
| Abstract | Cleidocranial dysplasia (CCD), an autosomal dominant disorder with a prevalence of 1 in 1,000,000 individuals, presents with a wide range of variability. Dentists are often the first to encounter patients with CCD, some of whom do not show typical manifestations. Since it has similar features to other pathologies, CCD is misdiagnosed as other conditions. A 10-year-old boy suffering from CCD was misdiagnosed as having rickets and was referred for non-eruption of a few permanent teeth along with an unaesthetic facial appearance. Clinically and radiologically, a diagnosis of CCD was made. Currently, management of this patient's orofacial manifestations is underway. |
| Volume Number | 2015 |
| e-ISSN | 1757790X |
| Journal | BMJ Case Reports |
| Language | English |
| Publisher | BMJ Publishing Group Ltd. |
| Publisher Place | Great Britain (UK) |
| Access Restriction | One Nation One Subscription (ONOS) |
| Subject Keyword | Cleidocranial Dysplasia Diagnosis Facies Rickets Tooth, Unerupted Brachydactyly Child Diagnosis, Differential Humans Male Surgery Case Reports Journal Article Multidisciplinary |
| Content Type | Text |
| Resource Type | Article |
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