DNA testing is available for a growing number of hereditary diseases in neurology and other specialities. In addition, DNA tests are important tools in the diagnosis of diseases, particularly in conditions for which clinical signs are relatively nonspecific. DNA testing also can provide valuable insight into the risk of hereditary disease when decisions about treating comorbidities are being made.
This panel is designed for individuals with a family history of neurological disorders or individuals with symptoms of the conditions, such as seizures, muscle weakness and cognitive impairment. Genetic testing can confirm a diagnosis and provide information related to a condition. Testing can also inform family planning decisions and provide reassurance for unaffected family members.
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