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

Abstract

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
Volume23
Issue number2
DOIs
StatePublished - Apr 1993

Fingerprint

Dive into the research topics of 'Schinzel-Giedion syndrome and congenital megacalyces'. Together they form a unique fingerprint.

Cite this