Your browser doesn't support javascript.
loading
A case of cerebrocostomandibular syndrome with congenital heart disease
Journal of the Korean Pediatric Society ; : 574-578, 1993.
Article in Korean | WPRIM | ID: wpr-88255
ABSTRACT
Cerebrocostomandibular syndrome is characterized by micrognathia, cleft palate, multiple thorax deformity and frequently, mental deficiency. Respiratory compromise is a common cause of death. We experienced a case of cerebrocostomandibular syndrome with congenital heart disease in a 2 day old female baby with the chief complaint of cyanosis and respiratory difficulty since birth. She was delivered by cesarian section due to delayed labor at IUP 42 weeks. The diagnosis was made on the basis of clinical features, radiologic findings and echocardiogram, which showed micrognathia, deformity of 3rd finger Lt, hemivertebrae of T1-T6 Lt., absence of 1-6th rib Lt., dextrocardia, tetralogy of fallot, atrial septal defect secondum. We reported this case and reviewed related litertures briefly.
Subject(s)

Full text: Available Index: WPRIM (Western Pacific) Main subject: Ribs / Congenital Abnormalities / Tetralogy of Fallot / Thorax / Cause of Death / Cleft Palate / Cyanosis / Parturition / Dextrocardia / Diagnosis Type of study: Diagnostic study Limits: Female / Humans Language: Korean Journal: Journal of the Korean Pediatric Society Year: 1993 Type: Article

Similar

MEDLINE

...
LILACS

LIS

Full text: Available Index: WPRIM (Western Pacific) Main subject: Ribs / Congenital Abnormalities / Tetralogy of Fallot / Thorax / Cause of Death / Cleft Palate / Cyanosis / Parturition / Dextrocardia / Diagnosis Type of study: Diagnostic study Limits: Female / Humans Language: Korean Journal: Journal of the Korean Pediatric Society Year: 1993 Type: Article