Vascular Ehlers-Danlos syndr. (MSA-WG)

Registry

The VASCERN Registry is an essential tool that offers a centralized repository for clinical data and information related to rare vascular diseases. By gathering clinical data, the registry aims to improve research, diagnosis, and care for patients. With standardized data collection and collaboration among healthcare professionals, researchers, and patients, the registry empowers personalized treatment, fosters innovation, and enhances patient care.

More information on the MSA-WG registry available on the Registry page here.

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