CLINICAL CASE OF STURGE-WEBER SYNDROME
Sturge-Weber syndrome is a neurocutaneous disorder that classically presents with a triad of vascular anomalies involving the skin, eyes, and brain. The disorder is caused by a postzygotic somatic gain of function of the GNAQ gene and, more recently, the GNA11 gene, which results in the characteristic clinical features. This article presents a clinical case of a patient with Sturge-Weber syndrome
Authors
- Nikita Belyakov (ORCID: https://orcid.org/0000-0002-9754-501X)
- V.V. Smirnova (ORCID: https://orcid.org/0000-0001-8021-0267)
- Irina Ivanovna Polikarpova
- Diana Vasilevna Ogureeva
- M.S. Shlyakhtin
Institutions
- Yaroslavl State Medical Academy (RU)
Publication Details
- Published
- 2025-05-28
- DOI
- https://doi.org/10.37539/250410.2025.41.61.015
- Primary Topic
- Vascular Malformations and Hemangiomas
- Type
- article
- Field-Weighted Citation Impact
- 0.00