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Austin Pathology
Test Directory
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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) ![]() |
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
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- |
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
|
Laboratory Instructions
|
None |
External Laboratory
|
Diagnostic Genomics, PathWest Laboratory Medicine |
Accredited Test
|
Yes |
These PDF documents can be downloaded for your reference