Cadasil
CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy) is a genetic disorder that affects the small vessels in the brain, causing strokes, dementia, and other neurological symptoms. It is caused by mutations in a gene called NOTCH3, located in chromosome 19. CADASIL is an important disorder to understand because it is the first disease to be linked to mutations in a gene involved in normal brain development. By understanding this disorder, researchers can better understand the causes of stroke, dementia, and other neurological diseases. Additionally, studying CADASIL can also help to develop therapeutic strategies for improving patient outcomes.
← Journal of DiseasesRelated Articles
1 journal(s) foundDiseases
ISSN: 2997-1977
Type: Open Access Journal
Editor: Andrzej Prystupa , Medical University of Lublin
Journal of Diseases is an international, multidisciplinary, peer-reviewed, open access, journal which aims to focus on the latest and outstanding research on diseases.