Sturge-Weber Syndrome Type III

Sturge-Weber syndrome (SWS) is a neurogenetic disease with an incidence of 1 in 20.000-50.000 live births. The less common form, which can be difficult to diagnose and only involves leptomeningeal angioma, has been defined as Type III SWS. A 5.5-month-old male patient with normal neuromotor developm...

Full description

Bibliographic Details
Main Authors: Hande Gazeteci Tekin, Sarenur Gökben, Sanem Yılmaz, Hasan Tekgül, Gül Serdaroğlu
Format: Article
Language:English
Published: Galenos Yayinevi 2018-06-01
Series:Journal of Pediatric Research
Subjects:
Online Access:http://jpedres.org/archives/archive-detail/article-preview/sturge-weber-syndrome-type-/19000