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Autosomal Recessive Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy 1
A CADASIL characterized by the onset of neurologic symptoms in infancy or early childhood that is caused by homozygous or compound heterozygous mutations in the NOTCH3 gene on chromosome 19p13.
This information is for educational purposes only and is not medical advice. Always consult your healthcare provider about your specific condition and treatment.
When to seek help
Seek medical help right away if you have severe, sudden, or worsening symptoms, trouble breathing, chest pain, or any symptom that feels life-threatening. This community is for peer support and education only and is not a substitute for professional medical advice.
If you are experiencing a medical emergency, contact your local emergency services immediately.
Overview
A CADASIL characterized by the onset of neurologic symptoms in infancy or early childhood that is caused by homozygous or compound heterozygous mutations in the NOTCH3 gene on chromosome 19p13.
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