Austin Pathology

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NOTCH3 gene testing (Blood)

Alternate Names
CADASIL, cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, NOTCH 3
Test Code
MISCSO
Testing Laboratory
Referred Laboratory
Specimen Type

Blood

Container Type

9 mL EDTA (Purple Top)

Container Image
Medicare Rebate

No - please complete Patient Financial Consent Form.pdf

Out of Pocket Costs
Please note: This service is not Medicare rebatable and patients may be charged. Out of Pocket cost - $1200
Fee above is an indication only; please contact testing laboratory for up-to date cost.
Ordering Information

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is the most common inheritable cause of stroke in patients before the age of 65. It is caused by mutations in the NOTCH3 gene. In addition to strokes, the clinical phenotype of CADASIL may include migraine, cognitive decline and psychiatric symptoms. It is recommended that patients be seen by a genetics service or specialist prior to requesting.

Collection Instructions

-

Transport Instructions
Transport ambient at room temperature
Storage Instructions
Store ambient at room temperature
Testing Frequency
Monday - Friday
Min Test Volume
2mL
Add On Test Suitability

Add ons for this test cannot be performed.

Container ID
EWP, EW, CR
CSR Instructions

WHOLE BLOOD SPECIMEN - DO NOT CENTRIFUGE.

Instructions for: Heidelberg Specimen Receptions

  • Place sample in Room Temperature Sendout tub
Laboratory Instructions
None
External Laboratory
Diagnostic Genomics, PathWest Laboratory Medicine
Accredited Test
Yes