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Dental Findings in Cornelia De Lange Syndrome

Date

2009

Author

Toker, Aslihan Soyal
Ay, Sinan
Yeler, Hasan
Sezgin, Ilhan

Metadata

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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.

Source

YONSEI MEDICAL JOURNAL

Volume

50

Issue

2

URI

https://dx.doi.org/10.3349/ymj.2009.50.2.289
https://hdl.handle.net/20.500.12418/10149

Collections

  • Makale Koleksiyonu [5200]
  • Makale Koleksiyonu [5745]
  • Öksüz Yayınlar Koleksiyonu - WoS [6162]



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