Klippel-Trenaunay-Weber syndrome with hemimegalencephaly; report of a pediatric case
Iranian Journal of Pediatrics. 2012; 22 (1): 137-141
en Inglés
| 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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Índice:
IMEMR (Mediterraneo Oriental)
Asunto principal:
Recién Nacido
/
Deformidades Congénitas del Pie
/
Mancha Vino de Oporto
/
Epilepsia Parcial Motora
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Síndromes Neurocutáneos
/
Malformaciones del Desarrollo Cortical
Tipo de estudio:
Informe de Casos
Límite:
Femenino
/
Humanos
Idioma:
Inglés
Revista:
Iran. J. Pediatr.
Año:
2012
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