Document Detail


Klippel-trenaunay-Weber syndrome with hydronephrosis and vesicoureteral reflux: an unusual association.
MedLine Citation:
PMID:  12026213     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The Klippel-Trenaunay-Weber syndrome is a rare disorder characterized by congenital vascular hamartomas, limb hypertrophy, cutaneous manifestations, lymphangiomas and atresia of lymph vessels with non-pitting edema. A three-year-old boy was referred to our clinic for progressive hypertrophy of leg and feet with 32-month history. We diagnosed Klippel-Trenaunay-Weber syndrome, and determined vesicoureteral reflux in our patient. To our knowledge, hydronephrosis and vesicoureteral reflux have not been described previously in the KTWS.
Authors:
Dinçer Yildizdaş; Bülent Antmen; Ibrahim Bayram; Hacer Yapicioğlu
Related Documents :
1620403 - The klippel-feil syndrome: implications for naval service.
15241163 - Klippel-feil syndrome: clinical features and current understanding of etiology.
8072053 - Munchausen's syndrome and substance abuse.
Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  The Turkish journal of pediatrics     Volume:  44     ISSN:  0041-4301     ISO Abbreviation:  Turk. J. Pediatr.     Publication Date:    2002 Apr-Jun
Date Detail:
Created Date:  2002-05-23     Completed Date:  2002-06-11     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  0417505     Medline TA:  Turk J Pediatr     Country:  Turkey    
Other Details:
Languages:  eng     Pagination:  180-2     Citation Subset:  IM    
Affiliation:
Department of Pediatrics, Cukurova University Faculty of Medicine, Adana, Turkey.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Child, Preschool
Humans
Hydronephrosis / complications*,  diagnosis
Klippel-Trenaunay-Weber Syndrome / complications*,  diagnosis
Male
Urography
Vesico-Ureteral Reflux / complications*,  diagnosis

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  The Mckusick-Kaufman syndrome: report of a case with some associations.
Next Document:  Analysis of the modifying effects of TAP 1/2 genes on cystic fibrosis phenotype.