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- Title
Klippel-Trenaunay Weber syndrome: A case report.
- Authors
Das, Subhashish
- Abstract
Highlights from the article: Klippel-Trenaunay Syndrome (KTS) is a rare congenital disorder due to a sporadic, autosomal dominant, or mosaic homozygosity mutation. Plain X-ray of long bones, computed tomography and magnetic resonance imaging contrast venography is essential ancillary tools along with a color-Doppler ultrasound, radiography, ascending phlebogram with or without contrast material are essential for the diagnosis of KTS.[[8]] Surgical treatment of venous malformations in Klippel-Trénaunay syndrome.
- Subjects
FIBRONECTINS; TURNER'S syndrome; SYNDROMES
- Publication
Medical Journal of Dr. D.Y. Patil Vidyapeeth, 2019, Vol 12, Issue 4, p359
- ISSN
2589-8302
- Publication type
Article
- DOI
10.4103/mjdrdypu.mjdrdypu_226_18