Journal of Indian Academy of Oral Medicine and Radiology (Jan 2018)

Cornelia de-Lange syndrome - A case report

  • Charvi Chawla,
  • Prasanna Kumar Rao,
  • Raghavendra Kini,
  • Devika Shetty

DOI
https://doi.org/10.4103/jiaomr.JIAOMR_153_16
Journal volume & issue
Vol. 30, no. 1
pp. 92 – 95

Abstract

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Cornelia de-Lange syndrome (CdLS) is a rare multisystem developmental disorder characterized by psychomotor retardation and delayed growth associated with a series of malformations, including facial dysmorphia, upper-extremity malformations, hirsutism, cardiac defects, and gastrointestinal abnormalities. There is no definitive biochemical or chromosomal marker for the prenatal diagnosis of syndrome so it is important for the clinician to know etiopathological aspects and characteristic features to provide health care and help improve the quality of life of affected individuals.

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