Information for Patients and Families
Familial Cavernous Malformations (CCM) - Common Hispanic Mutation
Sturge-Weber Syndrome (SWS) - Leptomeningeal Angiomatosis
Hereditary Hemorrhagic Telangiectasia (HHT) - Brain Arteriovenous Malformation (BAVM)
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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 > | ||||
