Ataxia Gene Panel

What is Ataxia Gene Panel test?

The Ataxia Gene Panel is a genetic test that analyzes multiple genes known to be associated with ataxia—a group of neurological disorders characterized by impaired coordination, balance, and speech. This panel helps identify genetic mutations that cause different types of hereditary ataxia, aiding in diagnosis and management.

Why consider Ataxia Gene Panel test?

• To diagnose the specific genetic cause of unexplained ataxia symptoms.
• To differentiate between various hereditary ataxias with overlapping clinical features.
• To guide treatment, management, and genetic counseling for patients and their families.
• To provide prognostic information and inform decisions about care and support.

Who should get tested for Ataxia Gene Panel test?

• Individuals experiencing symptoms of ataxia, such as unsteady gait, poor coordination, or speech difficulties.
• Patients with a family history of hereditary ataxia or related neurological disorders.
• Healthcare providers may recommend this test when clinical evaluation suggests a genetic cause of ataxia.

More Information about Ataxia Gene Panel test

OTHER NAMES: ataxia gene panel, Genetic ataxia testing, Spinocerebellar ataxia panel, Inherited Ataxia Gene Panel, Spinocerebellar Ataxia (SCA) Gene Panel, Comprehensive Ataxia NGS Panel

Spinocerebellar Ataxia is a group of inherited neurological disorders characterized by progressive problems with coordination and balance due to degeneration of the cerebellum and sometimes the spinal cord. Symptoms typically include difficulty walking, poor hand coordination, speech problems, and sometimes vision issues. Diagnosis is confirmed through genetic testing, often using panels like the Ataxia Gene Panel.