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Updated: Aug 9, 2026

Mutagenesis and Analysis of Genetic Mutations in the GC-rich KISS1 Receptor Sequence Identified in Humans with Reproductive Disorders
Published on: September 4, 2011
Goldston syndrome: report of a case
Y H Gulcan1, N Duman, A Kumral
1Department of Pediatrics, Dokuz Eylül University Faculty of Medicine, Izmir, Türkiye.
Abstract:
Cerebrohepatorenal malformation is a rare familial disorder characterized by typical renal lesions combined with Dandy-Walker malformation, and congenital hepatic fibrosis. In this case report, a male premie with the diagnosis of cerebrorenal syndrome or so called Goldston syndrome is presented. Besides the rarity of this syndrome, this case is the second reported patient diagnosed prenatally.
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