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An unusual variant of Klippel-Trenaunay syndrome. Association of total hemihypertrophy, hemimegalencephaly and bilateral extremity enlargement (case report).

作者信息

Cheruy M, Heller F R

出版信息

Acta Chir Belg. 1987 Mar-Apr;87(2):73-6.

PMID:3035842
Abstract

The case reported is the first description of an unusual form of Klippel-Trenaunay syndrome associating total hemihypertrophy to hemimegalencephaly and bilateral extremity enlargement. The patient complaints are related to her lower limb inequality; she presents dizziness, tinnitus and nystagmus which could be unusual consequences of hemimegalencephaly, disclosed at the EEG. Angiodysplasia is mild in regard to the hypertrophy whose cause is discussed.

摘要

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An unusual variant of Klippel-Trenaunay syndrome. Association of total hemihypertrophy, hemimegalencephaly and bilateral extremity enlargement (case report).
Acta Chir Belg. 1987 Mar-Apr;87(2):73-6.
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引用本文的文献

1
Klippel-trenaunay-weber syndrome with hemimegalencephaly; report of a pediatric case.伴有半侧巨脑症的克-特-韦综合征;一例儿科病例报告
Iran J Pediatr. 2012 Mar;22(1):147-51.
2
Hemimegalencephaly, hemihypertrophy and vascular lesions.半侧巨脑症、半侧肥大及血管病变。
Eur J Pediatr. 1995 Feb;154(2):134-7. doi: 10.1007/BF01991917.