Juvenile myasthenia gravis

Abstract

Juvenile myasthenia gravisJuvenile myasthenia gravis is a rare disorder acquired in childhood, representing 10% to 15% of all cases of myasthenia gravis. Like the adult form, it is generally characterized by an autoimmune attack on acetylcholine receptors at the neuromuscular junction. Most patients present with ptosis, diplopia, and fatigability. More advanced cases may also have bulbar problems and limb weakness and may progress to paralysis of the respiratory muscles. Abstract Access this article onlineWebsite: www.ijmedph.org