Limb-girdle myasthenia: Clinical, electrophysiological and morphological features in familial and autoimmune cases

C. Rodolico, A. Toscano, M. Autunno, S. Messina, C. Nicolosi, M. Aguennouz, M. Laurà, P. Girlanda, C. Messina, G. Vita

Research output: Contribution to journalArticlepeer-review

Abstract

Limb-girdle myasthenia is an uncommon disease and includes familial and autoimmune forms. Patients present proximal muscle weakness and wasting, and sometimes fatigability, without cranial nerve involvement and fluctuations. We observed, during a 15-year period, nine subjects with limb-girdle myasthenia, (24-55 years; 8 males, 1 female) who constituted 3.2% of 281 myasthenic patients attending our department. All had previously received a diagnosis different from myasthenia. Diagnosis of limb-girdle myasthenia was established by clinical, muscle biopsy and electrophysiological assessment including repetitive nerve stimulation and single fiber electromyography. Five patients had the familial form with tubular aggregates in skeletal muscle; four patients had the autoimmune form. Patients with the familial form had a good response to acetylcholinesterase inhibitors, and the patients with the autoimmune form responded to immunotherapy. Our findings reinforce the opportunity to suspect limb-girdle myasthenia in unclassifiable proximal myopathies and to differentiate familial from autoimmune cases, especially for therapeutic implications.

Original languageEnglish
Pages (from-to)964-969
Number of pages6
JournalNeuromuscular Disorders
Volume12
Issue number10
DOIs
Publication statusPublished - Dec 2002

Keywords

  • Limb-girdle weakness
  • Myasthenia
  • Tubular aggregates

ASJC Scopus subject areas

  • Clinical Neurology
  • Pediatrics, Perinatology, and Child Health
  • Developmental Neuroscience
  • Neurology

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