Interesting Case Epileptic Seizure as An Uncommon First Symptom in CADASIL with a Novel Likely Pathogenic Mutation Kesinee Katawatee, Pat Korathanakhu Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is the monogenic disease caused by the mutation of the gene on the chromosome 19 encoding the protein named NOTCH3. เมษายน - มิถุนายน 2566