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