The Goldston Syndrome: Report of a Case
- 1 January 1989
- journal article
- case report
- Published by Taylor & Francis in Pediatric Pathology
- Vol. 9 (3) , 337-343
- https://doi.org/10.3109/15513818909037738
Abstract
We present a case of the Goldston syndrome--that is, cystic renal dysplasia and the Dandy-Walker malformation. The condition was diagnosed by ultrasound in a 635 g fetus in the seventeenth week of gestation. Ultrasound studies showed the fetal head to be somewhat enlarged with slight dilatation of the lateral ventricles and marked dilatation of the fourth ventricle. The kidneys were symmetrically enlarged and multicystic. Autopsy revealed evidence of the oligohydramnios syndrome. The kidneys were typical of the Goldston syndrome as were the microscopic lesions in the liver. To our knowledge this is the first reported case in which this diagnosis was made during intrauterine life.Keywords
This publication has 3 references indexed in Scilit:
- Pathology of renal and hepatic anomalies in Meckel syndromeAmerican Journal of Medical Genetics, 1987
- THE DANDY-WALKER SYNDROMEJournal of Neuropathology and Experimental Neurology, 1963
- Correlation of Complications of Labor With Lesions in the Brains of NeonatesJournal of Neuropathology and Experimental Neurology, 1961