Movement Disorders + Hypotonia Panel is an 81-gene focused panel aimed at identifying the underlying genetic cause of movement disorder and congenital hypotonia.
| Test Code | 6867 |
| Turnaround Time (TAT) | 14-21 days |
| Number of Genes | 81 |
for all blood relatives of patients who undergo full single gene sequencing or multigene panel testing* at Ambry Genetics and are found to have a pathogenic or likely pathogenic variant. No-cost testing of blood relatives must be completed within 90 days of the original Ambry report date.
Order Now*excludes Secondary Findings and SNP Array tests
Patients with movement disorders and congenital hypotonia often undergo a diagnostic odyssey. For patients and families, this journey to an accurate diagnosis can be long and costly. Ambry Genetics can help facilitate early diagnosis which can help optimize disease management.
This test aims to identify genetic etiologies in patients with a clinical history involving movement disorders and hypotonia. This includes disorders such as aromatic L-amino acid decarboxylase (AADC) deficiency, several types of dystonias and dyskinesias, and other clinically overlapping conditions. Genes included are associated with one or more key clinical symptoms including congenital hypotonia and involuntary movement disorder.