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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