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Genet Couns ; 12(3): 263-7, 2001.
Article in English | MEDLINE | ID: mdl-11693790

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.


Subject(s)
Abnormalities, Multiple/genetics , Dandy-Walker Syndrome/genetics , Fetal Diseases/diagnosis , Polycystic Kidney Diseases/genetics , Prenatal Diagnosis , Abnormalities, Multiple/diagnostic imaging , Adult , Brain/abnormalities , Dandy-Walker Syndrome/diagnostic imaging , Female , Humans , Infant, Newborn , Karyotyping , Liver Cirrhosis/congenital , Lung/abnormalities , Male , Nervous System Malformations/pathology , Polycystic Kidney Diseases/pathology , Pregnancy , Syndrome , Ultrasonography
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