Congenital Horner syndrome: A rare though significant complication of subclavian flap aortoplasty

Journal of Thoracic and Cardiovascular Surgery

Volumn 120, Issue 2, 2000, Pages 419-421

  Naimer, Sody Abby ^a,b,c   Weinstein, Orly ^a,b,c   Rosenthal, Gidon ^a,b,c  

^a Goosh Katif Family Health Center   (Israel)

^b BEN GURION UNIVERSITY OF THE NEGEV   (Israel)

^c BEN GURION UNIVERSITY OF THE NEGEV   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

AORTOPLASTY; ARTICLE; CASE REPORT; DOPPLER ECHOGRAPHY; ECHOCARDIOGRAPHY; FEMALE; HORNER SYNDROME; HUMAN; HUMAN CELL; HUMAN TISSUE; NEWBORN; PRIORITY JOURNAL; SUBCLAVIAN ARTERY; SURGICAL ANATOMY; SURGICAL TECHNIQUE;

EID: 0033863199     PISSN: 00225223     EISSN: None     Source Type: Journal    
DOI: 10.1067/mtc.2000.107340     Document Type: Article

References (6)

1. Pancoast's syndrome
2. Brown-Sequard syndrome
3. Congenital Horner's syndrome
4. Turner's syndrome occurring with Horner's syndrome
5. Late results of the subclavian flap repair of coarctation in infancy
6. Surgical treatment of aortic coarctation in infants younger than three months: 1985 to 1990. Success of extended end-to-end arch aortoplasty