Broad diagnostic approach for all types of movement disorders considered for study, regardless of age. This includes paroxysmal movement disorders of metabolic origin, parkinsonism, chorea, calcification of the basal ganglia, and cerebral iron accumulation disease.
It depends on the disease subgroup.
Large panel covering a heterogeneous group of disorders. Genetic diagnosis allows family counseling, prognosis, and treatment.
Clinical suspicion of movement disorder.
General panel
How to order
1. Download & fill out
Please cover as many fields as possible in both documents
2. Sample collection
Three sample types: saliva, peripheral blood or genomic DNA
3. Pack the sample
Please pack the sample in a way to prevent leakage
4. Send the sample & the request
Please schedule the delivery for Monday–Friday: 8am – 5pm
5. Result: the report
Via: e-mail and/or through the customer portal
"*" indicates required fields
Turnaround time (TAT): 25 days
Ref. S-202008659
Large panel covering a heterogeneous group of disorders. Genetic diagnosis allows family counseling, prognosis and treatment. In addition to including all the genes already present in each of the specific panels, some other genes belonging to rarer conditions and with more complex phenotypes have been included. We highlight the inclusion in this panel of:
Priority Genes : Genes where there is sufficient evidence (clinical and functional) to consider them associated with the disease; they are included in the clinical practice guidelines.
Secondary Genes: Genes related to the disease, but with a lower level of evidence or that constitute sporadic cases.
* Candidate Genes: Not enough evidence in humans, but potentially associated with the disease.
