X-linked Charcot-Marie-Tooth disease and progressive-relapsing central demyelinating disease

Neurology. 2005 Nov 22;65(10):1672-3. doi: 10.1212/01.wnl.0000186032.06791.94.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Brain / pathology*
  • Brain / physiopathology
  • Brain Stem / pathology
  • Brain Stem / physiopathology
  • Cerebellum / pathology
  • Cerebellum / physiopathology
  • Charcot-Marie-Tooth Disease / complications*
  • Charcot-Marie-Tooth Disease / genetics
  • Connexins / genetics
  • DNA Mutational Analysis
  • Diagnosis, Differential
  • Disease Progression
  • Gap Junction beta-1 Protein
  • Genetic Diseases, X-Linked / diagnosis
  • Genetic Diseases, X-Linked / genetics*
  • Genetic Diseases, X-Linked / physiopathology
  • Genetic Predisposition to Disease / genetics*
  • Genetic Testing
  • Hereditary Central Nervous System Demyelinating Diseases / diagnosis*
  • Hereditary Central Nervous System Demyelinating Diseases / genetics*
  • Hereditary Central Nervous System Demyelinating Diseases / physiopathology
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Methylprednisolone / therapeutic use
  • Multiple Sclerosis / diagnosis
  • Multiple Sclerosis / physiopathology
  • Mutation / genetics
  • Oligoclonal Bands / cerebrospinal fluid
  • Recurrence
  • Treatment Failure

Substances

  • Connexins
  • Oligoclonal Bands
  • Methylprednisolone