Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Klippel-Trénaunay-Weber syndrome.

J R Nielsen1, E H Tschen

  • 1Department of Dermatology, University of New Mexico School of Medicine, Albuquerque.

Cutis
|July 1, 1987
PubMed
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.

Related Experiment Videos

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

SARS-CoV-2 in first trimester pregnancy: a cohort study.

Human reproduction (Oxford, England)·2020
Same author

Airway plans and capnography.

Anaesthesia·2019
Same author

Correction.

Anaesthesia·2018
Same author

Difficult mask ventilation and muscle relaxation.

Anaesthesia·2018
Same author

Objective description of mask ventilation.

British journal of anaesthesia·2016
Same author

The diet of whiting Merlangius merlangus in the western Baltic Sea.

Journal of fish biology·2016

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.