Document Detail


Schinzel-Giedion syndrome and congenital megacalyces.
MedLine Citation:
PMID:  8516031     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
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.
Authors:
T E Herman; D A Sweetser; W H McAlister; S B Dowton
Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Pediatric radiology     Volume:  23     ISSN:  0301-0449     ISO Abbreviation:  Pediatr Radiol     Publication Date:  1993  
Date Detail:
Created Date:  1993-07-22     Completed Date:  1993-07-22     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  0365332     Medline TA:  Pediatr Radiol     Country:  GERMANY    
Other Details:
Languages:  eng     Pagination:  111-2     Citation Subset:  IM    
Affiliation:
Mallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, Missouri 63110.
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MeSH Terms
Descriptor/Qualifier:
Abnormalities, Multiple*
Bone and Bones / abnormalities
Face / abnormalities
Humans
Hydronephrosis / congenital
Infant
Kidney Calices / abnormalities*,  ultrasonography
Syndrome

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