Sturge Weber syndrome in a multinational pediatric cohort: a systematic analysis of different types
Abstract Background Sturge-Weber Syndrome (SWS) is characterized by leptomeningeal capillary malformation (CM), glaucoma, and facial vascular birthmark. The Roach Scale differentiates between cases with facial birthmark (Roach Type I) versus isolated brain involvement (Type III). Most previous studi...
Saved in:
| Main Authors: | Sigrid Disse, Georgia Ramantani, Hanna Küpper, Annette Bock, Georg-Christoph Korenke, Birgit Weidner, Martin Preisel, Regina Trollmann, Adelheid Wiemer-Kruel, Sven Wellmann, Knut Brockmann, Simone Schroeder, Sascha Meyer |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
BMC
2025-07-01
|
| Series: | Orphanet Journal of Rare Diseases |
| Subjects: | |
| Online Access: | https://doi.org/10.1186/s13023-025-03769-2 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Sturge-Weber Syndrome: A comprehensive review of clinical features, optimized diagnosis and management strategies
by: Katarzyna Naja, et al.
Published: (2024-12-01) -
Epilepsy in Sturge-Weber syndrome: a literature review and description of a clinical case
by: N. I. Shova, et al.
Published: (2020-04-01) -
A Review of Sturge–Weber Syndrome Brain Involvement, Cannabidiol Treatment and Molecular Pathways
by: Katharine Elizabeth Joslyn, et al.
Published: (2024-11-01) -
Predicting and Preventing Epilepsy in Sturge-Weber Syndrome?
by: Csaba Juhász
Published: (2016-11-01) -
Ocular Manifestations of the Sturge–Weber Syndrome
by: Kiana Hassanpour, et al.
Published: (2021-07-01)