[123I]FP-CIT SPECT findings in two patients with Hallervorden-Spatz disease with homozygous mutation in PANK2 gene

Neurology. 2005 Jan 11;64(1):167-8. doi: 10.1212/01.WNL.0000148577.62644.77.
No abstract available

MeSH terms

  • Adult
  • Female
  • Homozygote
  • Humans
  • Iodine Radioisotopes*
  • Male
  • Mutation / genetics*
  • Pantothenate Kinase-Associated Neurodegeneration / diagnosis*
  • Pantothenate Kinase-Associated Neurodegeneration / enzymology
  • Pantothenate Kinase-Associated Neurodegeneration / genetics*
  • Phosphotransferases (Alcohol Group Acceptor) / genetics*
  • Siblings
  • Tomography, Emission-Computed, Single-Photon / methods*

Substances

  • Iodine Radioisotopes
  • Phosphotransferases (Alcohol Group Acceptor)
  • pantothenate kinase