Abstract

Two cases of familial myasthenia gravis are reported. One patient is a typical case of autoimmune myasthenia with positive anti acetylcholine receptor antibodies, while in the second patient the impairment of neuromuscular transmission is likely to be due to antibodies directed against determinants other than the acetylcholine receptors.
Lingua originaleEnglish
pagine (da-a)1228-1230
Numero di pagine3
RivistaJOURNAL OF NEUROLOGY, NEUROSURGERY AND PSYCHIATRY
Volume51
Stato di pubblicazionePubblicato - 1988

Keywords

  • Adult
  • Autoantibodies
  • Humans
  • Male
  • Middle Aged
  • Myasthenia Gravis
  • Neuromuscular Junction
  • Receptors, Cholinergic

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