A clinician's dilemma: Sturge-Weber syndrome 'without facial nevus'!!

Abstract:

:Sturge-Weber syndrome (SWS) is a rare, sporadic neurocutaneous syndrome characterized by a classical triad of facial port wine nevus, ipsilateral leptomeningeal angiomatosis (LAM) and glaucoma. The incidence of SWS is 1/50,000 live births, although it is more often underreported. The incidence of SWS without facial nevus is not known, although very few patients without facial nevus have been reported. In these patients, the diagnosis of SWS is made by the findings of computed tomography, magnetic resonance imaging, and histopathology. Here, we report three patients with SWS from our cohort of 28 patients with SWS without facial nevus and discuss their clinical profile and outcome.

journal_name

Ann Indian Acad Neurol

authors

Jagtap SA,Srinivas G,Radhakrishnan A,Harsha KJ

doi

10.4103/0972-2327.107725

subject

Has Abstract

pub_date

2013-01-01 00:00:00

pages

118-20

issue

1

eissn

0972-2327

issn

1998-3549

pii

AIAN-16-118

journal_volume

16

pub_type

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