Please use this identifier to cite or link to this item: http://dspace.sctimst.ac.in/jspui/handle/123456789/10492
Title: Sturge-Weber Syndrome: Clinical Spectrum, Disease Course, and Outcome of 30 Patients
Authors: Jagtap, S
Srinivas, G
Harsha, KJ
Radhakrishnan, N
Radhakrishnan, A
Keywords: Neurosciences & Neurology; Pediatrics
Issue Date: 2013
Publisher: JOURNAL OF CHILD NEUROLOGY
Citation: 28 ,6;722-728
Abstract: Sturge-Weber syndrome is a heterogeneous neurocutaneous syndrome with facial and leptomeningeal angiomas, glaucoma, seizures, stroke-like episodes, and mental retardation. The authors critically evaluated the clinical manifestations, outcome, and natural history in 30 patients with Sturge-Weber syndrome followed up from January 1985 to May 2010. Of the patients, 15 were males, age at diagnosis ranged from 1 month to 43 years. Typical port-wine stain nevus occurred in 26 (86%), it was bilateral in 2 (8%), and it was absent in 4 (4%). Nine patients had glaucoma (30%), 3 required surgery. Four had transient hemiparesis. All patients had seizures; they were well controlled in 22 (73.3%); in 8 they remained drug resistant. Three patients underwent surgery and became seizure-free. Of the 17 who had mental subnormality, 14 (82.4%) had seizure onset before 2 years. An early age at seizure onset and those with drug-resistant seizures had more severe degree of mental subnormality. Uncontrolled seizures, mental subnormality, visual handicap, and cosmetic disfiguration were the major impediments in life.
URI: 10.1177/0883073812451326
http://dspace.sctimst.ac.in/jspui/handle/123456789/10492
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