Klippel-Trénaunay-Weber Syndrome: A Case Report.
Klippel-Trénaunay-Weber syndrome: A Case Report.
DOI:
https://doi.org/10.70284/njirm.v7i6.1408Keywords:
Klippel–Trénaunay–Weber syndrome, colour doppler, lower limbAbstract
Klippel–Trénaunay–Weber syndrome is a syndrome combination of capillary malformations, soft-tissue or bone hypertrophy, and varicose veins or venous malformations. Most cases are considered sporadic. However, some of the possible differential diagnoses may have familial predispositions. We report one such case having right leg A-V malformation presented with complain of varicosity and non healing ulcer. [Arun G NJIRM 2016; 7(6):119-120]
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2. Copel J. Obstetric Imaging, Elsevier Health Sciences. (2012)
3. Dhir L, Quinn AG. Persistent fetal vasculature and spontaneous hyphema in a patient with Klippel-Trénaunay-Weber syndrome. J AAPOS. 2010;14(2):190-2.
4. Servelle M. Klippel and Trenaunay's syndrome. 768 operated cases. Ann Surg Mar. 1985;201(3):365–73.
5. Cha SH, Romeo MA, Neutze JA. Visceral manifestations of Klippel-Trénaunay syndrome. Radiographics.25(6):1694-7doi:10.1148/rg.256055042
6. Phadke SR: Klippel Trenaunay syndrome. Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2009;13(2):153-155
7. Marler JJ, Fishman SJ, Upton J et-al. Prenatal diagnosis of vascular anomalies. J. Pediatr. Surg. 2002;37 (3): 318-26.
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Published
2018-02-08
How to Cite
Gaur, A. K., Modi, B., & Mehta, S. (2018). Klippel-Trénaunay-Weber Syndrome: A Case Report.: Klippel-Trénaunay-Weber syndrome: A Case Report. National Journal of Integrated Research in Medicine, 7(6), 119–120. https://doi.org/10.70284/njirm.v7i6.1408
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Case Report
