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: Migraine headachesStrokes—may have multiple strokesMental health issues, such as depression or anxietySeizuresMemory problemsConfusion
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
Your bodily fluids may be tested. This can be done with: A skin biopsyGenetic tests
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: MigrainesDepression or anxietyCognitive difficulties
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: Get support from family members and friends. Talk to them about your diagnosis.Consider a support group for people with genetic disorders.Become educated. Learn about CADASIL and ways that you can stay healthy.
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.
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 4, 2014. Accessed November 12, 2014.
Fan Y, McGowan S, Rubeiz H, et al. Acute encephalopathy as the initial manifestation of CADASIL. Neurol Clin Pract. 2012;2(4):359-361.
NOTCH3 gene. Genetics Home Reference website. Available at:
http://ghr.nlm.nih.gov/gene/NOTCH3. Published November 4, 2014. Accessed November 12, 2014.
What is CADASIL? CADASIL Foundation website. Available at:
http://cadasilfoundation.org/what.html. Accessed November 12, 2014.
Last reviewed November 2015 by Rimas Lukas, MD
Please be aware that this information is provided to supplement the care provided by your physician. It is neither intended nor implied to be a substitute for professional medical advice. CALL YOUR HEALTHCARE PROVIDER IMMEDIATELY IF YOU THINK YOU MAY HAVE A MEDICAL EMERGENCY. Always seek the advice of your physician or other qualified health provider prior to starting any new treatment or with any questions you may have regarding a medical condition.
Copyright © EBSCO Publishing. All rights reserved.