Klippel-Trenaunay Syndrome
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Learn About Klippel-Trenaunay Syndrome

What is the definition of Klippel-Trenaunay Syndrome?

Klippel-Trenaunay syndrome (KTS) is a rare condition that is typically present at birth. The syndrome often involves port wine stains, excess growth of bones and soft tissue, and varicose veins.

What are the alternative names for Klippel-Trenaunay Syndrome?

Klippel-Trenaunay-Weber syndrome; KTS; Angio-osteohypertrophy; Hemangiectasia hypertrophicans; Nevus verucosus hypertrophicans; Capillary-lymphatico-venous malformation (CLVM)

What are the causes of Klippel-Trenaunay Syndrome?

KTS is caused by a genetic variation that occurs during fetal development. Why this occurs is unknown.

What are the symptoms of Klippel-Trenaunay Syndrome?

Symptoms of KTS include:

  • Many port wine stains or other blood vessel problems, including dark spots on the skin
  • Varicose veins (may be seen in early infancy, but are more likely to be seen later in childhood or adolescence)
  • Unstable gait due to limb-length difference (involved limb is longer)
  • Bone, vein, or nerve pain

Other possible symptoms:

  • Bleeding from the rectum
  • Blood in the urine
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What are the support groups for Klippel-Trenaunay Syndrome?

More information and support for people with KTS and their families can be found at:

  • K-T Support Group -- k-t.org
  • Vascular Birthmarks Foundation -- birthmark.org
What is the outlook (prognosis) for Klippel-Trenaunay Syndrome?

Most people with KTS do well, although the condition may affect their appearance.

Who are the top Klippel-Trenaunay Syndrome Local Doctors?
Elite in Klippel-Trenaunay Syndrome
Pediatric Radiology
Elite in Klippel-Trenaunay Syndrome
Pediatric Radiology

Department Of Radiology

300 Longwood Ave, 
Boston, MA 
Languages Spoken:
English

Ahmad Alomari is a Pediatric Radiologist in Boston, Massachusetts. Dr. Alomari is rated as an Elite provider by MediFind in the treatment of Klippel-Trenaunay Syndrome. His top areas of expertise are Klippel-Trenaunay Syndrome, Arteriovenous Malformation, Parkes Weber Syndrome, Blue Rubber Bleb Nevus Syndrome, and Septoplasty.

Elite in Klippel-Trenaunay Syndrome
Dermatology | Pediatrics
Elite in Klippel-Trenaunay Syndrome
Dermatology | Pediatrics

Mayo Clinic

200 1st St Sw, 
Rochester, MN 
Languages Spoken:
English
Accepting New Patients

Megha Tollefson is a Dermatologist and a Pediatrics provider in Rochester, Minnesota. Dr. Tollefson is rated as an Elite provider by MediFind in the treatment of Klippel-Trenaunay Syndrome. Her top areas of expertise are Klippel-Trenaunay Syndrome, Progressive Hemifacial Atrophy, Vascular Birthmark, and Hemangioma. Dr. Tollefson is currently accepting new patients.

 
 
 
 
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Sarah C. Contrucci
Experienced in Klippel-Trenaunay Syndrome
Experienced in Klippel-Trenaunay Syndrome

St. Christopher's Pediatric Associates Radiology - E. Erie Avenue

160 E Erie Ave, 
Philadelphia, PA 
Languages Spoken:
English

. Dr. Contrucci is rated as an Experienced provider by MediFind in the treatment of Klippel-Trenaunay Syndrome. Her top areas of expertise are Tracheobronchopathia Osteoplastica, Scoliosis, Short Stature (Growth Disorders), and Familial Short Stature (FSS).

What are the latest Klippel-Trenaunay Syndrome Clinical Trials?
A Phase 2 Study of Mutant-selective PI3Kα Inhibitor, RLY-2608, in Adults and Children With PIK3CA Related Overgrowth Spectrum and Malformations Driven by PIK3CA Mutation

Summary: This is a 3-part Phase 2 randomized study evaluating the safety and efficacy of the mutant-selective PI3Kα inhibitor, RLY-2608, in adults and children with PIK3CA Related Overgrowth Spectrum (PROS) and malformations driven by PIK3CA mutation. Part 1 is a dose selection, Part 2 is a basket design with exploratory single-arm cohorts for various subpopulations of participants, and Part 3 is randomize...

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Lymphatic Anomalies Registry for the Assessment of Outcome Data

Summary: Lymphatic anomalies are a rare subset of vascular anomalies that are poorly understood. the understanding of the natural history, long-term outcomes, risk factors for morbidity and mortality, and the relative benefit of medical therapies and procedures is limited.The goal of this project is to better understand these diseases and improve the care of theses rare patients. To do this, the investigat...

Who are the sources who wrote this article ?

Published Date: October 27, 2025
Published By: Anna C. Edens Hurst, MD, MS, Associate Professor in Medical Genetics, The University of Alabama at Birmingham, Birmingham, AL. Review provided by VeriMed Healthcare Network. Also reviewed by David C. Dugdale, MD, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team.

What are the references for this article ?

Greene AK, Mulliken JB. Vascular anomalies. In: Losee JE, Hopper RA, eds. Plastic Surgery: Volume 3: Craniofacial, Head and Neck Surgery and Pediatric Plastic Surgery. 5th ed. Philadelphia, PA: Elsevier; 2024:chap 31.

K-T Support Group website. Clinical practice guidelines for Klippel-Trenaunay syndrome (KTS). k-t.org/assets/images/content/BCH-Klippel-Trenaunay-Syndrome-Management-Guidelines-1-6-2016.pdf. Updated January 6, 2016. Accessed December 18, 2025.

McCormick AA, Grunwaldt LJ. Vascular anomalies. In: Zitelli BJ, McIntire SC, Nowalk AJ, Garrison J, eds. Zitelli and Davis' Atlas of Pediatric Physical Diagnosis. 8th ed. Philadelphia, PA: Elsevier; 2023:chap 10.

Rausch AC, Longman RE. Klippel-Trenaunay-Weber syndrome. In: Copel JA, D'Alton ME, Feltovich H, et al, eds. Obstetric Imaging: Fetal Diagnosis and Care. 3rd ed. Philadelphia, PA: Elsevier; 2026:chap 138.