Article
Sturge-Weber Syndrome in a Multinational Paediatric Cohort: A Systematic Analysis of Different Types
2025-02-07
Abstract excerpt
<title>Abstract</title> <p>Background Sturge-Weber Syndrome (SWS) is a rare neurocutaneous disease, characterized by cerebral capillary-venous malformation, glaucoma, and facial vascular birthmark. Different types are reflected in the Roach classification. Most previous studies have focussed on classic SWS Type I, but Type III cases, lacking facial birthmark, were mostly described in case reports. We systematica...
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Identifiers and source
- Literature Corpus work
- da08432b-cf95-5801-a495-69355bb24558
- DOI
- 10.21203/rs.3.rs-5890276/v1
