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Sturge-Weber syndrome: A case study.

Linda D Welty
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Abstract

Sturge-Weber syndrome (SWS) is a rare, sporadic, progressive, congenital syndrome. In its complete trisymptomatic form, SWS is physically characterized by port-wine stains over the trigeminal area, leptomeningeal angiomas usually over the parieto-occipital region, and eye abnormalities. Clinical manifestation for infants with SWS depends on the affected organs, but can include seizures, mental retardation, and glaucoma. This article begins with a case presentation of an infant with SWS and then presents the etiology, embryology, pathophysiology, clinical presentation, management, and prognosis of SWS.

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Diagnosis, DifferentialDisease ProgressionFemaleGlaucomaHumansIncidenceInfant, NewbornIntensive Care, NeonatalInternetMagnetic Resonance ImagingNeonatal NursingNurse's RoleParentsPatient Care TeamPhysical ExaminationPrognosisRare DiseasesSeizuresSocial SupportSturge-Weber SyndromeCase ReportsJournal ArticleReview

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Linda D Welty. Sturge-Weber syndrome: A case study.. https://doi.org/10.1891/0730-0832.25.2.89

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