Glomerulomegaly in a Patient With Cyanotic Congenital Heart Disease
- 1 July 1970
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of Pediatrics & Adolescent Medicine
- Vol. 120 (1) , 69-71
- https://doi.org/10.1001/archpedi.1970.02100060103017
Abstract
A 17-year-old boy developed proteinuria nine years after he underwent a Potts-Smith-Gibson procedure as treatment for hypoplastic right ventricle, pulmonary stenosis, and tricuspid atresia. The only abnormality found to account for the proteinuria was glomerulomegaly, a benign lesion previously undescribed in living subjects.Keywords
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