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The diagnosis of SWS generally relies upon the finding
of a typical facial port-wine stain associated with a leptomeningeal
angioma and/or glaucoma. The majority of patients with SWS will
have skin involvement, however a small subset of patients have
been identified who have the typical neurologic or ophthalmologic
manifestations but lack the port-wine stain. This section will
cover the neurologic, ophthalmologic, and dermatologic evaluations
and tests recommended to make the diagnosis of Sturge-Weber Syndrome
and screen for its associated complications.
Dermatologic
Evaluation
Neurologic
Evaluation
Ophthalmologic
Evaluation |
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