Juvenile limb-girdle myasthenia gravis

Carmelo Rodolico, C. Pastura, S. Sinicropi, P. Girlanda, A. Toscano, C. Messina, G. Vita

Research output: Contribution to journalArticlepeer-review

Abstract

Limb-girdle myasthenia is a rare disorder which includes familial and autoimmune forms. Myasthenia gravis is an uncommon disease in children and its diagnosis may be difficult. We report here five cases of autoimmune juvenile LGM starting before the age of 16 years with attention to clinical diagnostic difficulties, evolution, laboratory and instrumental data as well as response to treatment. Diagnosis of limb-girdle myasthenia requires a strong index of suspicion also in childhood. We suggest that this form be suspected in children with unclassifiable myopathy, mostly affecting deltoid muscles and lower extremities.

Original languageEnglish
Pages (from-to)353-356
Number of pages4
JournalNeuropediatrics
Volume36
Issue number6
DOIs
Publication statusPublished - Dec 2005

Keywords

  • Juvenile
  • Limb-girdle myasthenia

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Clinical Neurology

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