Dental Findings in Cornelia De Lange Syndrome |
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| Authors: | Aslihan Soyal Toker Sinan Ay Hasan Yeler Ilhan Sezgin |
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| Affiliation: | 1Department of Oral and Maxillofacial Surgery, Faculty of Dentistry, Cumhuriyet University, Sivas, Turkey.;2Department of Oral and Maxillofacial Surgery, Faculty of Dentistry, Gaziantep University, Gaziantep, Turkey.;3Department of Medical Biology and Genetics, Faculty of Medicine, Cumhuriyet University, Sivas, Turkey. |
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| Abstract: | Cornelia de Lange syndrome is a congenital disease, basically characterized by psychomotor retardation associated with a series of malformations, including mainly skeletal, craniofacial deformities together with gastrointestinal and cardiac malformations. There is no definitive biochemical or chromosomal marker for the prenatal diagnosis of this syndrome. We actually want to present the case of a 10-year-old patient, who was admitted to our clinic for dental pain. The patient had the symptoms of Cornelia de Lange syndrome. During the oral examination of this patient, the patient was found to have the typical symptoms of Cornelia de Lange syndrome, such as micrognathia and delayed eruption in conjunction with the symptoms of the Hutchinson''s syndrome, which had never been reported before. |
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| Keywords: | Cornelia de Lange Brachmann de Lange syndrome Hutchinson''s teeth dental caries |
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