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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Klippel-trenaunay-Weber syndrome with hydronephrosis and vesicoureteral reflux: an unusual association.

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.[1]

References

  1. Klippel-trenaunay-Weber syndrome with hydronephrosis and vesicoureteral reflux: an unusual association. Yildizdaş, D., Antmen, B., Bayram, I., Yapicioğlu, H. Turk. J. Pediatr. (2002) [Pubmed]
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