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83. The Invitae Dystonia Panel analyzes up to 23 genes associated with the dystonias, a group of movement disorders characterized by sustained muscle contractions that lead to abnormal postures and repetitive movements. These genes were curated based on available evidence to provide a comprehensive test for the monogenic causes of dystonia, including both isolated and combined dystonias. Dystonias are a heterogeneous group of disorders. Identification of the molecular basis of disease can be useful in confirming a diagnosis, predicting disease course, and informing recurrence risk. Preliminary evidence genes currently have early evidence of a clinical association with the specific disease covered by this test. Some clinicians may wish to include genes which do not currently have a definitive clinical association, but which may prove to be clinically significant in the future. These genes can be added at no additional charge. Visit our Preliminary evidence genes page to learn more. Preliminary evidence genes currently have early evidence of a clinical association with the specific disease covered by this test. Some clinicians may wish to include genes which do not currently have a definitive clinical association, but which may prove to be clinically significant in the future.



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