You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1, look for clinical trials, and connect with others living with it — all in one place.
Open the full Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1 hub →Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1 is a rare condition. Also known as Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy, Hereditary multi-infarct dementia. Tomeko brings together the specialists, research, clinical trials, treatments and community for Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:136 · OMIM 125310 · ICD-10 I67.8 · GARD 0001049
Start by learning the basics from an authoritative source, find a specialist or center that sees Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1, and connect with a patient organization. Tomeko brings these together on one hub.
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1, filtered to your area.
Tomeko shows live, recruiting studies for Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1 from ClinicalTrials.gov on the hub.