Sturge-Weber Syndrome clinical trials at UCSF

1 research study open to eligible people

Sturge-Weber syndrome is a rare condition present at birth that affects the skin, brain, and eyes. UCSF is running studies that follow people over time to find brain markers linked to seizures and stroke-like events. Study tests include MRI scans, blood samples, and neurological exams to track changes.

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  • Longitudinal Studies to Identify Biomarkers for Sturge-Weber Syndrome

    open to all eligible people

    Individuals with Sturge-Weber Syndrome (SWS) sometimes have brain involvement which can result in seizures, stroke-like episodes and neurologic deficits. The purpose of this study is to integrate longitudinal clinical data, radiological data, and blood biomarkers of Sturge-Weber syndrome patients. The research aims are: 1. To integrate longitudinal clinical data, radiological data, and blood biomarkers of Sturge-Weber syndrome patients. 2. Identify plasma and imaging biomarkers sensitive to exacerbation of clinical symptoms including seizures, headaches, or stroke-like episodes. 3. For enrolled patients who present with severe neurological symptoms screen blood samples for inflammatory changes. The target enrollment for this study is about 250 individuals diagnosed with Sturge-Weber Syndrome. The goal of this study is to understand more about Sturge-Weber Syndrome, the possible treatments for this disease, and identify targets for clinical trials. Those participating in the database will be asked to consent to blood draws.

    San Francisco, California and other locations

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