OUTSOURCE
NOTCH3 MUTATION DETECTION; CADASIL (N174)
Also Known As:
NOTCH 3 Mutation Detection
CADASIL
About This Test
Autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a progressive disorder of the small arterial vessels of the brain, manifested as migraine, strokes, and white matter lesions, with resultant cognitive impairment in some patients. Autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1 (CADASIL1) is caused by heterozygous mutations in the NOTCH3 gene on chromosome 19p13. The disorder is characterized by relapsing strokes with neuropsychiatric symptoms and affects relatively young adults of both sexes. This test is useful for hot spot mutation screening of exon 3, 4, 5 and 6 of the NOTCH3 gene.
Test Parameters (1)
- NOTCH3 MUTATION DETECTION; CADASIL
Home Collection
✓ Available
Reports Available In
1 Day
Frequently Asked Questions
Outsourced test are being done from Dr. Lal Path Lab. Charges and reporting time is same as of Dr. Lal Path Labs.
Physician prescription is mandatory.
NOTCH3 Mutation Detection (CADASIL test) is important because it helps confirm the diagnosis of CADASIL, a hereditary disorder affecting small blood vessels of the brain.
TAT Policy
The Turnaround Time (TAT) depends on the following factors:
- Registration date and time
- Type of scan or test
- Scan time or sample collection time
In uncommon circumstances, TAT may be delayed due to test complexity or reasons beyond our control. You will be informed of the estimated TAT at the time of registration.
