Journal
YONSEI MEDICAL JOURNAL
Volume 50, Issue 2, Pages 289-292Publisher
YONSEI UNIV COLL MEDICINE
DOI: 10.3349/ymj.2009.50.2.289
Keywords
Cornelia de Lange; Brarchmann de Lange; syndrome; Hutchinson's teeth; dental caries
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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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