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Original Article
A Case of Cornelia de Lange syndrome.
Byoung Hong Ahn, Song Nyeon Choi, Young Wook Kim, Ki Bok Kim
Clin Exp Pediatr. 1990;33(2):234-240.   Published online February 28, 1990
We have experienced a case of Cornelia de Lange syndrome in a 3-year-old boy. The patient showed most of the typical clinical features of the syndrome: microcephaly, bushy eyebrows and synophys, antimongolian slant, small nose and anteverted nostrils, thin protruding lips with downturning of the comer, micrognathia, low set ears, generalized hirsuitism, and growth redardation. The patient also had skeletal abnormalities of hands. Chromosomal...
A Case of Cornelia de Lange Syndrome.
Hwa Kyoung Oh, Soo Jung Yoo, Myung Jin Kim, Mi Na Lee
Clin Exp Pediatr. 1990;33(1):94-99.   Published online January 31, 1990
We have experienced a case of Cornelia de Lange syndrome in a girl of 4.5/12 years old. She showed typical features of a microbrachycephaly, hirsuitism and characteristic face with bushy eyebrows, antimongolian slant depressed nasal bridge, thin protruding lips with downtuming of the comers and the microtia. She also had severe retardation in growth and mental development. The diagnosis was established by typical clinical...
A Case of Cornelia de Lange Syndrome.
Jung Han, Soo Taek Bae, Soon Ok Byun, Ji Sub Oh
Clin Exp Pediatr. 1988;31(2):282-287.   Published online February 28, 1988
The Cornelia de Lange syndrome is characterized by severe growth and mental retardation, typical face, and low-pitched, weak, growling cry, as was first described by Cronelia de Lange in 1933. We have recognized a case of Cornelia de Lange syndrome in a 4 month old Korean girl. The patient showed typical appearance of face with low forehead, bushy eyebrows and synophrys, long curly eyelases,...
Case Report
A Case of Cornelia De Large Syndrome.
Do Seung Lee, Dae Young Hwang, Jeong Sick Min, Jae Sun Park
Clin Exp Pediatr. 1983;26(6):616-621.   Published online June 30, 1983
We have experienced a case of1 Cornelia de Lange Syndrome in a male infant. At first visit, the patient showed typical appearance of microcephaly, cleft palate, generalized hirsutism and growth retardation due to poor sucking since birth. The face of the patient was characterized by micrognathia, antirrongolism slant of eyes, synorphys of eye brows, bushy forehead and bushy lateral aspect of both cheeks, all...
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