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Klippel-Trenaunay-Weber syndrome with hemimegalencephaly; report of a pediatric case
Iranian Journal of Pediatrics. 2012; 22 (1): 137-141
in English | IMEMR | ID: emr-124371
ABSTRACT
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. 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. Occurrence of partial motor seizures in addition to bilateral lower extremities extensive port-wine staining is a unique feature seen in our case
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Index: IMEMR (Eastern Mediterranean) Main subject: Infant, Newborn / Foot Deformities, Congenital / Port-Wine Stain / Epilepsy, Partial, Motor / Neurocutaneous Syndromes / Malformations of Cortical Development Type of study: Case report Limits: Female / Humans Language: English Journal: Iran. J. Pediatr. Year: 2012

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Index: IMEMR (Eastern Mediterranean) Main subject: Infant, Newborn / Foot Deformities, Congenital / Port-Wine Stain / Epilepsy, Partial, Motor / Neurocutaneous Syndromes / Malformations of Cortical Development Type of study: Case report Limits: Female / Humans Language: English Journal: Iran. J. Pediatr. Year: 2012