Neurological manifestations in two related xeroderma pigmentosum group D patients: complications of the late-onset type of the juvenile form

Mov Disord. 1997 Jul;12(4):616-9. doi: 10.1002/mds.870120428.
No abstract available

Publication types

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

MeSH terms

  • Adult
  • Age of Onset
  • Atrophy
  • Cerebellar Ataxia / diagnosis
  • Cerebellar Ataxia / genetics*
  • Cerebellar Ataxia / physiopathology
  • Cerebellum / pathology
  • Child
  • Disease Progression
  • Female
  • Humans
  • Magnetic Resonance Imaging
  • Movement Disorders / diagnosis
  • Movement Disorders / genetics*
  • Movement Disorders / physiopathology
  • Nerve Degeneration / genetics
  • Xeroderma Pigmentosum / complications*
  • Xeroderma Pigmentosum / genetics
  • Xeroderma Pigmentosum / physiopathology