Cerebellar hypometabolism with normal structural findings in Cerebrotendinous xanthomatosis. A case report

Clin Neurol Neurosurg. 2015 Dec:139:221-3. doi: 10.1016/j.clineuro.2015.10.020. Epub 2015 Oct 17.
No abstract available

Keywords: 18FDG PET; Autosomal recessive disorder; Cerebellum; Cerebrotendinous xanthomatosis; Spastic paraparesis.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Cerebellum / metabolism*
  • Female
  • Fluorodeoxyglucose F18*
  • Humans
  • Positron-Emission Tomography
  • Radiopharmaceuticals*
  • Xanthomatosis, Cerebrotendinous / diagnosis*
  • Xanthomatosis, Cerebrotendinous / genetics

Substances

  • Radiopharmaceuticals
  • Fluorodeoxyglucose F18