| Literature DB >> 6486955 |
C A Bullaboy, W M Derkac, D H Johnson, R B Jennings.
Abstract
A 4 1/2-month-old infant was referred to our center with the rare combination of tetralogy of Fallot and coarctation of the aorta. Despite the presence of severe right ventricular outflow obstruction, the infant was virtually acyanotic because of the systemic afterload associated with the coarctation. She had marked systemic hypertension. The embryological and therapeutic implications of this child's defects are discussed.Entities:
Mesh：
Year: 1984 PMID： 6486955 DOI： 10.1016/s0003-4975(10)62294-1
Source DB: PubMed Journal: Ann Thorac Surg ISSN： 0003-4975 Impact factor: 4.330