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

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Klippel-Trénaunay-Weber syndrome.

The Klippel-Trénaunay-Weber syndrome is a congenital angiodysplasia most often characterized by a triad of symptoms: varicose veins, port-wine cutaneous hemangiomas, and symmetrical hypertrophy of the affected limb. We report a case in a 37-year-old man and present a review of the literature.[1]

References

  1. Klippel-Trénaunay-Weber syndrome. Nielsen, J.R., Tschen, E.H. Cutis; cutaneous medicine for the practitioner. (1987) [Pubmed]
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