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Genetic and Rare Diseases Information Center (GARD)

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Cerebrotendinous xanthomatosis


Other Names for this Disease

  • Cerebral cholesterinosis
  • CTX
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.

Your Question

I believe my daughter may have cerebrotendinous xanthomatosis. Can you provide me with more information on this condition?

Our Answer

We have identified the following information that we hope you find helpful. If you still have questions, please contact us.

What is cerebrotendinous xanthomatosis?

Cerebrotendinous xanthomatosis is a type of lipid storage disease. Symptoms of this condition include diarrhea in infants, cataracts in children, tendon xanthomas, and progressive neurologic dysfunction. It is caused by mutations in the CYP27A1 gene. Treatment may involve chenodeoxycholic acid (CDCA), inhibitors of HMG-CoA reductase, and surgery to remove cataracts.[1]
Last updated: 9/12/2013

What are the signs and symptoms of cerebrotendinous xanthomatosis?

The symptoms associated cerebrotendinous xanthomatosis are listed below, including the typical age when each symptom appears.[1]
Last updated: 9/12/2013

Where do the xanthomas typically occur?

The xanthomas commonly occur on the tendons, such as the Achilles tendon and the tendons of the elbows, hands, knees, and neck. Xanthomas have also been reported in the lungs, bones, and central nervous system.[1]
Last updated: 9/12/2013

What causes cerebrotendinous xanthomatosis?

Cerebrotendinous xanthomatosis is caused by mutations in the CYP27A1 gene. This condition is inherited in an autosomal recessive pattern.[1]
Last updated: 9/12/2013

Is genetic testing available for cerebrotendinous xanthomatosis?

Yes, testing of the CYP27A1 gene is available. The Genetic Testing Registry provides information on clinical and research tests available for this condition.
Last updated: 9/12/2013

How is cerebrotendinous xanthomatosis diagnosed?

Cerebrotendinous xanthomatosis is diagnosed by a combination of clinical features, cholestanol levels, and genetic testing. Individuals with cerebrotendinous xanthomatosis have high levels of cholestanol in their blood. Genetic testing of the CYP27A1 gene is also available and can detect mutations in about 98% of patients.[1]
Last updated: 9/12/2013

How might cerebrotendinous xanthomatosis be treated?

Cerebrotendinous xanthomatosis may be treated with chenodeoxycholic acid (CDCA), which has been shown to normalize levels of cholestonal and improve neurologic symptoms. Inhibitors of HMG-CoA reductase may be used alone or in combination with CDCA. They are also effective in decreasing cholestanol concentration and improving clinical symptoms, however these treatments can induce muscle damage. Coenzyme Q10 may improve muscle weakness, and cataract surgery may also be required.[1]
Last updated: 10/17/2013

References
Other Names for this Disease
  • Cerebral cholesterinosis
  • CTX
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.