Report of a newborn with hemimegalencephaly in association with Klippel-Trenaunay-Weber syndrome

Klippel-Trenaunay-Weber syndrome (KTW) is a rare phacomatosis whose main characteristics are: cutaneous angiomas (vascular nevi), varicose veins (arteriovenous fistulae) and hemihypertrophy of bones and soft tissues. This is a case report of KTW syndrome which was diagnosed in the first days of life...

Full description

Bibliographic Details
Main Authors: Obradović Slobodan, Vuletić Biljana, Stojković-Anđelković Anđelka, Igrutinović Zoran
Format: Article
Language:English
Published: Serbian Medical Society 2005-01-01
Series:Srpski Arhiv za Celokupno Lekarstvo
Subjects:
Online Access:http://www.doiserbia.nb.rs/img/doi/0370-8179/2005/0370-81790502062O.pdf