Hypoglossal neuropathy in hereditary neuropathy with liability to pressure palsy

Neurology. 2003 Oct 28;61(8):1154-5. doi: 10.1212/01.wnl.0000086808.56096.da.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Chromosomes, Human, Pair 17 / genetics
  • DNA Mutational Analysis
  • Female
  • Genetic Predisposition to Disease
  • Humans
  • Hypoglossal Nerve Diseases / complications*
  • Hypoglossal Nerve Diseases / diagnosis
  • Hypoglossal Nerve Diseases / physiopathology
  • Myelin Proteins / genetics
  • Nervous System Diseases / complications*
  • Nervous System Diseases / diagnosis
  • Nervous System Diseases / genetics
  • Paralysis / etiology*
  • Pressure / adverse effects
  • Remission, Spontaneous
  • Sequence Deletion
  • Tongue / physiopathology

Substances

  • Myelin Proteins
  • PMP22 protein, human