Format

Send to

Choose Destination
Turk J Pediatr. 2011 May-Jun;53(3):337-41.

Prenatally detected congenital cystic adenomatoid malformation and postnatally diagnosed trisomy 13: case report and review of the literature.

Author information

1
Division of Neonatology, Department of Pediatrics, Gazi University, Faculty of Medicine, Ankara, Turkey.

Abstract

Congenital cystic adenomatoid malformation (CCAM) is a rare bronchopulmonary malformation characterized by loss of the normal pulmonary tissue. CCAM may be frequently associated with cardiac and renal anomalies. Rarely, CCAM may be seen with chromosome abnormalities. This is the first reported neonatal case of prenatally detected CCAM and postnatally diagnosed trisomy 13.

PMID:
21980820
[Indexed for MEDLINE]

Supplemental Content

Loading ...
Support Center