Three cases of Cornelia de Lange syndrome.
- Author:
Sang Min SEONG
1
;
Jun Sung LEE
;
Dong Bock LEE
;
Kyung Tai WHANG
Author Information
1. Department of Pediatrics, Catholic Medical College, Seoul, Korea.
- Publication Type:Case Report
- MeSH:
Chromosome Aberrations;
De Lange Syndrome*;
Diagnosis;
Female;
Forehead;
Hirsutism;
Humans;
Infant;
Lip;
Nose
- From:Journal of the Korean Pediatric Society
1978;21(3):232-238
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
We have experienced 3 cases of Cornelia de Lange syndrome in Korean female infants. They showed typical clinical features of a microbrachycephaly, hirsutism and characteristic face with low forehead bushy eye brows, antimongolian slant, large and depressed briedge of nose, thin protruding lips with down turning of the corners and micrognathia. They also had skeletal abnormalities and chromosomal abnormalities. The diagnosis was established by clinical, laboratory and X-ray findings. The brief review of literature was made.
