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Klippel-Trenaunay-Weber syndrome
J G Meine1, R A Schwartz, C K Janniger
1New Jersey Medical School, Newark 07103-2714, USA.
Cutis
|October 7, 1997
Summary
Klippel-Trenaunay-Weber syndrome presents with a port-wine stain, varicose veins, and limb overgrowth. Early diagnosis and management are crucial for minimizing complications in affected infants and children.
Area of Science:
- Vascular Malformations
- Genetics
- Pediatric Medicine
Background:
- Klippel-Trenaunay-Weber syndrome (KTWS) is a rare congenital disorder.
- It is characterized by a triad of port-wine stains, venous malformations, and hypertrophy of soft tissues and bone.
Purpose of the Study:
- To review the clinical features, etiology, assessment, and treatment of Klippel-Trenaunay-Weber syndrome.
- To emphasize the importance of early recognition and intervention.
Main Methods:
- Literature review of clinical features, etiology, assessment, and treatment modalities.
- Synthesis of current knowledge on Klippel-Trenaunay-Weber syndrome.
Main Results:
- KTWS presents with a distinct triad of vascular and limb abnormalities.
- Early identification allows for timely management to reduce potential morbidity.
Conclusions:
- Klippel-Trenaunay-Weber syndrome requires a multidisciplinary approach for optimal patient outcomes.
- Further research into the genetic basis and novel treatment strategies is warranted.