Klippel-Trenaunay-Weber Syndrome with Hemimegalencephaly; Report of a Pediatric Case

被引：0
作者：
Esmailzadeh, Hossein [1 ]
Tavassoli, Azita [1 ]
Jahangiri, Younes [2 ]
Vatankhah, Nasibeh [2 ]
机构：
[1] Univ Tehran Med Sci, Aliasghar Pediat Ctr, Sch Med, Tehran, Iran
[2] Univ Tehran Med Sci, Med Educ & Dev Ctr, Tehran, Iran
来源：
IRANIAN JOURNAL OF PEDIATRICS | 2012年 / 22卷 / 01期
关键词：
Klippel-Trenaunay-Weber Syndrome; Hemimegalencephaly; Neurocutaneous Syndrome; HEMIHYPERTROPHY; MALFORMATION; INHERITANCE;
D O I：
暂无
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
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.
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页码：137 / 141
页数：5
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