SCOUT BY MIRUM: MOVEMENT DISORDERS GENETIC PANEL
Mirum Pharmaceuticals Offers a No-Cost Movement Disorders Genetic Panel for patients*
Mirum has partnered with PreventionGenetics, a College of American Pathologists-accredited laboratory†
Criteria for No-Cost CTX Testing
*Program may be canceled or changed at any time.
†Note that Mirum Pharmaceuticals cites the above-named external testing resource for information purposes only, and does not endorse or guarantee in any way the services or advice provided by them.
Any questions can be addressed by the PreventionGenetics genetic counselors and staff at (715) 387-0484.
COMPREHENSIVE
GENE PANEL TO HELP DIAGNOSE GENETIC CAUSES OF MOVEMENT DISORDERS
Sample collection INSTRUCTIONS
Buccal swab collection flyer
Download and share this buccal swab collection flyer.
While you may choose to collect a sample in your office, kits that help patients collect and ship their buccal samples can also be sent directly to their homes.
If you’d like to give your patients printed instructions with detailed illustrations, you can download and share this collection flyer. These instructions will also be included in the test kit that is sent directly to the patient’s home.
Educational patient brochure
To provide your patients with overall information about CTX and the genetic test, download and share this patient brochure. This brochure will also be included in the test kit that is sent directly to the patient’s home.
SCOUT BY MIRUM: MOVEMENT DISORDERS GENETIC PANEL
Reference:
- Stelten BM. Cerebrotendious xanthomatosis: a treatable inborn error of metabolism. Dissertation. Donders series 598. Radboud University. March 13, 2023. Accessed April 19, 2024. https://repository.ubn.ru.nl/handle/2066/289601