AI Article Synopsis
- Congenital cystic adenomatoid malformation (CCAM) is a rare lung condition where normal lung tissue is missing.
- CCAM can be linked with heart and kidney problems, and in rare cases, chromosome anomalies.
- This case study highlights the first known instance of a newborn with CCAM that was detected before birth, along with a diagnosis of trisomy 13 after birth.
Article 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.
Download full-text PDF |
Source |
|---|
Publication Analysis
Top Keywords
prenatally detected
8
congenital cystic
8
cystic adenomatoid
8
adenomatoid malformation
8
postnatally diagnosed
8
diagnosed trisomy
8
detected congenital
4
malformation postnatally
4
trisomy case
4
case report
4
Similar Publications
Want AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!