Rutgers Cancer Institute of New Jersey
195 Little Albany Street
New Brunswick, NJ 08903-2681
CADASIL is a genetic disorder that affects the brain. A gene mutation affects the muscle cells surrounding small blood vessels in the brain. The muscles cause damage to these blood vessels. It can reduce blood flow. This can lead to migraines, strokes, and dementia.
Copyright © Nucleus Medical Media, Inc.
CADASIL is caused by a mutation on the NOTCH3 gene. This gene is found on chromosome 19.
The main risk factor is having a parent with this disorder.
For some people with CADASIL, symptoms develop around age 30. Others do not have symptoms until much later in life.
These symptoms may include:
You will be asked about your symptoms and medical history. It will focus on whether or not your parents or another family member has or had CADASIL or early onset strokes, dementia, seizures, or migraines. A physical exam will be done.
Images may be taken of your brain. This can be done with an MRI scan.
Your bodily fluids may be tested. This can be done with:
Researchers are studying ways to treat CADASIL. If you are diagnosed with this disorder, your doctor will work closely with you to create a treatment plan.
Treatment is focused on relieving your symptoms. This may include medication to treat:
Other medications may be given to reduce your risk of a stroke or heart attack. These may include daily aspirin or medication to lower blood pressure.
When prescribing medication, your doctor will be careful. Certain drugs can worsen your condition by reducing blood flow in your brain.
Being diagnosed with CADASIL is a life-changing event. It is normal to have a range of emotions as a result. To help manage this change:
There is no known way to prevent this disorder. But if you have a family history of CADASIL, you can talk with a genetic counselor when deciding to have children.
Genetics Home Reference
Heart and Stroke Foundation of Canada
Bersano A, Bedini G, Oskam J, et al. CADASIL: treatment and management options. Curr Treatment Options Neurol. 2017;19(9):31.
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. Genetics Home Reference website. Available at: http://ghr.nlm.nih.gov/condition/cerebral-autosomal-dominant-arteriopathy-with-subcortical-infarcts-and-leukoencephalopathy. Published November 7, 2017. Accessed November 10, 2017.
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). EBSCO DynaMed Plus website. Available at:http://www.dynamed.com/topics/dmp~AN~T474352/Cerebral-autosomal-dominant-arteriopathy-with-subcortical-infarcts-and-leukoencephalopathy-CADASIL. Updated June 7, 2017. Accessed November 10, 2017.
Fan Y, McGowan S, Rubeiz H, et al. Acute encephalopathy as the initial manifestation of CADASIL. Neurol Clin Pract. 2012;2(4):359-361.
Migraine in adults EBSCO DynaMed Plus website. Available at:http://www.dynamed.com/topics/dmp~AN~T114718/Migraine-in-adults. Updated August 9, 2016. Accessed November 10, 2017.
NOTCH3 gene. Genetics Home Reference website. Available at: http://ghr.nlm.nih.gov/gene/NOTCH3. Published November 7, 2017. Accessed November 10, 2017.
Stroke rehabilitation. EBSCO DynaMed Plus website. Available at:http://www.dynamed.com/topics/dmp~AN~T580145/Stroke-rehabilitation. Updated April 10, 2017. Accessed November 10, 2017.
What is CADASIL? CADASIL Foundation website. Available at: http://cadasilfoundation.org/what.html. Accessed November 10, 2017.
Last reviewed November 2018 by EBSCO Medical Review Board Rimas Lukas, MD Last Updated: 12/20/2014