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Iranian Journal of Pediatrics
Tehran University of Medical Sciences Press
ISSN: 1018-4406
EISSN: 2008-2150
Vol. 22, No. 1, 2012, pp. 137-141
Bioline Code: pe12025
Full paper language: English
Document type: Case Report
Document available free of charge

Iranian Journal of Pediatrics, Vol. 22, No. 1, 2012, pp. 137-141

 en Klippel-Trenaunay-Weber Syndrome with Hemimegalencephaly; Report of a Pediatric Case
Esmailzadeh, Hossein; Tavassoli, Azita; Jahangiri, Younes & Vatankhah, Nasibeh


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 portwine staining is a unique feature seen in our case.

Klippel-Trenaunay-Weber Syndrome; Hemimegalencephaly; Neurocutaneous Syndrome

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