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What is Klippel-Trenaunay syndrome mean?
Klippel–Trénaunay syndrome, formerly Klippel–Trénaunay–Weber syndrome and sometimes angioosteohypertrophy syndrome and hemangiectatic hypertrophy, is a rare congenital medical condition in which blood vessels and/or lymph vessels fail to form properly. The three main features are nevus flammeus (port-wine stain), venous and lymphatic malformations, and soft-tissue hypertrophy of the affected limb. It is similar to, though distinctly separate from, the less common Parkes Weber syndrome.
The classical triad of Klippel–Trenaunay syndrome consists of:
vascular malformations of the capillary, venous and lymphatic vessels;varicosities of unusual distribution, particularly the lateral venous anomaly; andunilateral soft and skeletal tissue hypertrophy, usually the lower extremity. referencePosted on 17 Nov 2024, this text provides information on Miscellaneous in Medical related to Medical. Please note that while accuracy is prioritized, the data presented might not be entirely correct or up-to-date. This information is offered for general knowledge and informational purposes only, and should not be considered as a substitute for professional advice.
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