Innovative Journal of Pediatrics
The Scientific Journal of Growth & Development Research Center
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Klippel-Trenaunay-Weber Syndrome with Hemimegalencephaly; Report of a Pediatric Case
Author(s):
1Medical Education & Development Center, Tehran University of Medical Sciences, Tehran, Iran
2Aliasghar Pediatric Center, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
3Medical Education and Development Center, Tehran University of Medical Sciences, Tehran, Iran
*Corresponding Author: Medical Education and Development Center, Tehran University of Medical Sciences, Tehran, Iran Email: [email protected]
Published online:Mar 31, 2012
Article type:Case Report
Received:Jul 21, 2010
Accepted:Jun 02, 2011
How to Cite:Jahangiri Y, Tavassoli A, Esmailzadeh H, Vatankhah N. Klippel-Trenaunay-Weber Syndrome with Hemimegalencephaly; Report of a Pediatric Case. Inn J Pediatr. 2016;22(1):. doi:
Abstract
Background: Klippel-Trenaunay-Weber Syndrome (KTWS) is a rare neurocutaneous syndrome. Hemimegalencephaly (HME) and seizure episodes have been reported previously in a few cases with KTWS.
Case Presentation: We report here a 3 day-old girl with partial motor seizures, extensive port-wine staining and mild structural deformities in the feet, and a hemimegalencephaly.
Conclusion: Occurrence of partial motor seizures in addition to bilateral lower extremities extensive port-wine staining is a unique feature seen in our case.
References
- 1.References are available in PDF.
Copyright
© 2016, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.
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