Cerebrotendinous xanthomatosis: a rare disease with diverse manifestations

Arch Neurol. 2002 Apr;59(4):527-9. doi: 10.1001/archneur.59.4.527.

Abstract

This mini-review deals with a new appraisal of cerebrotendinous xanthomatosis. In addition to neurologic symptoms, patients with cerebrotendinous xanthomatosis develop cataracts, diarrhea, Achilles tendon xanthoma, atherosclerotic vascular disease, and many other abnormalities. Although the pathophysiology of the disease is not completely understood, excess production and consequent accumulation of cholestanol in tissues may play a crucial role. Chenodeoxycholic acid is the most effective therapy. The causative role and detrimental effects (at a low plasma level) of cholestanol merit further investigation.

Publication types

  • Review

MeSH terms

  • Brain Diseases / diagnosis*
  • Brain Diseases / drug therapy
  • Brain Diseases / metabolism
  • Brain Diseases / physiopathology
  • Chenodeoxycholic Acid / therapeutic use*
  • Cholestanol / metabolism*
  • Diagnosis, Differential
  • Humans
  • Hyperlipoproteinemia Type II / diagnosis
  • Musculoskeletal Diseases / diagnosis
  • Sitosterols / blood
  • Tendons* / physiopathology
  • Xanthomatosis / diagnosis*
  • Xanthomatosis / drug therapy
  • Xanthomatosis / metabolism
  • Xanthomatosis / physiopathology

Substances

  • Sitosterols
  • Chenodeoxycholic Acid
  • gamma-sitosterol
  • Cholestanol