Chylothorax and respiratory distress in a newborn with trisomy 21

European Journal of Pediatrics

Volumn 160, Issue 12, 2001, Pages 744-745

  Turan, Özden ^a   Canter, Berna ^a   Ergenekon, Ebru ^a  

^a GAZI UNIVERSITY   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME ABERRATION; CHYLOTHORAX; CLINICAL FEATURE; CYANOSIS; DIAGNOSTIC TEST; DISEASE ASSOCIATION; FACIES; HUMAN; LABORATORY TEST; MALE; NEWBORN; PATHOGENESIS; PHYSICAL EXAMINATION; PLEURA EFFUSION; PRIORITY JOURNAL; RESPIRATORY DISTRESS; TACHYPNEA; TRISOMY 21;

EID: 0035209935     PISSN: 03406199     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004310100842     Document Type: Article

References (8)

1. Spontaneous neonatal chylothorax. Apropos of 5 cases
2. Congenital chylothorax in a trisomy 21 newborn
3. Chylothorax in Down syndrome associated with hydrops fetalis
4. Congenital non-chylous pleural effusion with Down's syndrome
5. Variable levels of mosaicism for trisomy 21 in a non-immune hydropic infant with chylothorax
6. Trisomy 21 presented as a transient unilateral pleural effusion at 18 weeks' gestation
7. Congenital chylothorax in a patient with 21 trisomy syndrome
8. Chylothorax in two mongoloid infants