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Klippel-Trénaunay-Weber syndrome
1Department of Dermatology, University of New Mexico School of Medicine, Albuquerque.
Cutis
|July 1, 1987
Summary
Klippel-Trénaunay-Weber syndrome, a congenital angiodysplasia, presents with varicose veins, port-wine hemangiomas, and limb hypertrophy. This case report details a 37-year-old male patient, offering insights into this rare condition.
Area of Science:
- Vascular Medicine
- Dermatology
- Genetics
Background:
- Klippel-Trénaunay-Weber syndrome is a rare congenital vascular malformation.
- It typically manifests as a triad of port-wine stains, venous malformations, and bony or soft tissue hypertrophy.
- Accurate diagnosis and management are crucial for patient outcomes.