Vascular Ehlers-Danlos Syndrome: Current Understanding and Treatment Strategies
Vascular Ehlers-Danlos Syndrome (vEDS) is a rare and severe subtype of Ehlers-Danlos Syndrome (EDS), a group of inherited disorders affecting connective tissue. Unlike other EDS subtypes primarily characterized by joint hypermobility and skin elasticity, vEDS is distinguished by its impact on the vascular system, posing a significant risk of life-threatening complications1. This review aims to provide a concise overview of vEDS, encompassing its genetic basis, clinical manifestations, diagnostic approaches, and current treatment strategies.
Authors
- Erik D. Foehr (ORCID: https://orcid.org/0000-0002-7595-5632)
- Reece M. Foehr
Publication Details
- Journal
- Journal of Rare Diseases Research & Treatment
- Published
- 2025-04-16
- DOI
- https://doi.org/10.29245/2572-9411/2025/1.1217
- Primary Topic
- Vascular Tumors and Angiosarcomas
- Type
- article
- Field-Weighted Citation Impact
- 0.00