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In Depth:
Familial Cavernous Malformations (CCM)
Common Hispanic Mutation
Sturge-Weber Syndrome (SWS)
Leptomeningeal Angiomatosis
Hereditary Hemorrhagic Telangiectasia (HHT)
Brain Arteriovenous Malformation
(BAVM)
Finding Answers: How can I Contribute to the BVMC
Refer patients to the Contact Registry
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The Brain Vascular Malformations Consortium is a part of NIH Rare Diseases Clinical Research Network (RDCRN). Funding and/or programmatic support for this project has been provided by the National Institute of Neurological Disorders and Stroke (NINDS) and the NIH Office of Rare Diseases Research (ORDR). Read Disclaimer > |
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