Early-Onset Acquired Myasthenia Gravis Secondary to Anti-Muscle-Specific Kinase Autoantibodies

Articles > Article · 2012

Authors: Sanem KESKİN YILMAZ, SARENUR GÖKBEN, GÜL AKTAN, Ayfer AKÇAY

JOURNAL OF CHILD NEUROLOGY, Journal Indexed in SCI Expanded, International, 2012, vol 29, pp 108-110

DOI: 10.1177/0883073812467689

Summary

Autoimmune myasthenia gravis is rarely seen during infancy. Similar to adults, 85% to 90% of generalized pediatric myasthenia gravis cases have acetylcholine receptor antibodies. Approximately 30% of the remaining cases have antibodies against muscle-specific kinase. Information on the clinical course, treatment alternatives, and prognosis of pediatric muscle-specific kinase antibody-positive myasthenia gravis is limited because of the small number of cases. Here, we present a 14-month-old girl with muscle-specific kinase antibody-positive myasthenia gravis as one of the youngest patients described so far in the literature.

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