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Tests and diagnosis

By Mayo Clinic staff

Besides conducting a physical exam and a neurological exam, including checking your memory and concentration, vision, hearing, balance, coordination and reflexes, your doctor may request these laboratory tests:

  • Blood tests. Certain blood tests can confirm or exclude the suspected condition. A sample of your blood will be drawn from your arm through a needle. You may be required to fast from midnight the night before your appointment until after your blood is drawn. The specific tests will depend on the suspected cause, but most likely will include a complete blood count (CBC), which helps evaluate your overall health and detect a range of disorders, including infection and heavy metal poisoning.
  • Urine tests. Examining a sample of your urine under a microscope (urinalysis) may suggest certain systemic abnormalities that can be related to some forms of ataxia. If your doctor suspects Wilson's disease, you may be asked for a 24-hour urine collection to help determine the amount of copper in your system.
  • Imaging studies. A computerized tomography (CT) scan or magnetic resonance imaging (MRI) of your brain may help determine potential causes.
  • Lumbar puncture (spinal tap). A needle is inserted into your lower back (lumbar region) between two lumbar bones (vertebrae) to remove a sample of cerebrospinal fluid. The fluid, which surrounds and protects your brain and spinal cord, is sent to a laboratory for testing.
  • Genetic testing. Your doctor may recommend genetic testing to determine whether you or your child has the gene mutation that causes one of the hereditary ataxic conditions. Gene tests are available for many but not all of the hereditary ataxias.
References
  1. NINDS ataxias and cerebellar or spinocerebellar degeneration information page. National Institute of Neurological Disorders and Stroke. http://www.ninds.nih.gov/disorders/ataxia/ataxia.htm. Accessed Dec. 9, 2010.
  2. Frequently asked questions about Fredreich's ataxia (FRDA). National Ataxia Foundation. http://www.ataxia.org/resources/publications.aspx. Accessed Dec.30, 2010.
  3. Paulson HL. The spinocerebellar ataxias. Journal of Neuro-Opthalmology. 2009;29:227.
  4. Frequently asked questions about episodic ataxia. National Ataxia Foundation. http://www.ataxia.org/resources/publications.aspx. Accessed Dec. 9, 2010.
  5. Klockgether T. Sporadic ataxia with adult onset: Classification and diagnostic criteria. The Lancet Neurology. 2010;9:94.
  6. Ataxia-Telangiectasia (A-T). National Ataxia Foundation. http://www.ataxia.org/resources/publications.aspx. Accessed Dec. 9, 2010.
  7. Ataxia telangiectasia: Fact sheet. National Cancer Institute. http://www.cancer.gov/cancertopics/factsheet/ataxiaqa. Accessed Dec. 9, 2010.
  8. Opal P, et al. Overview of the hereditary ataxias. http://www.uptodate.com/home/index.html. Accessed Nov. 22, 2010.
DS00910 March 1, 2011

© 1998-2013 Mayo Foundation for Medical Education and Research (MFMER). All rights reserved. A single copy of these materials may be reprinted for noncommercial personal use only. "Mayo," "Mayo Clinic," "MayoClinic.com," "EmbodyHealth," "Enhance your life," and the triple-shield Mayo Clinic logo are trademarks of Mayo Foundation for Medical Education and Research.

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