Schinzel-Giedion syndrome and congenital megacalyces

T. E. Herman, D. A. Sweetser, W. H. McAlister, S. B. Dowton

Research output: Contribution to journalArticlepeer-review

23 Scopus citations


The Schinzel-Giedion syndrome is a rare autosomal recessive condition with typical facies, skeletal manifestations and congenital hydronephrosis. We report an infant with characteristic findings who had bilateral congenital megacalyces. Congenital megacalyces is believed to be a developmental abnormality, occurs in other malformation syndromes and has not previously been described in the Schinzel-Giedion syndrome.

Original languageEnglish
Pages (from-to)111-112
Number of pages2
JournalPediatric radiology
Issue number2
StatePublished - Apr 1 1993


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