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 language | English |
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Pages (from-to) | 111-112 |
Number of pages | 2 |
Journal | Pediatric radiology |
Volume | 23 |
Issue number | 2 |
DOIs | |
State | Published - Apr 1993 |