Email this article 2 cases transformation myasthenia gravis to amyotrophic lateral sclerosis
- Authors: Sanadze A.G.1, Kasatkina L.F.1
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Affiliations:
- Moscow Myasthenia Center
- Issue: Vol 2, No 4 (2012)
- Pages: 53-58
- Section: CLINICAL DISCUSSION
- Published: 21.11.2012
- URL: https://nmb.abvpress.ru/jour/article/view/99
- DOI: https://doi.org/10.17650/2222-8721-2012-0-4-53-58
- ID: 99
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Abstract
A72-year old woman and 38-year old man had clinical sings of myasthenia gravis with ptosis and double vision, speech, swallowing, face and limb weakness. They was diagnosed MG after tensilon test, responding to piridostigmine and prednisolon treatment, neuromuscular
disorders and positive anti-AchR and titin antibodies. Four and 7 year ago after debut of myasthenia gravis they had clinical and electrophysiological symptoms of amyotrophic lateral sclerosis.
About the authors
A. G. Sanadze
Moscow Myasthenia Center
Author for correspondence.
Email: ag-sanadze@mail.ru
Russian Federation
L. F. Kasatkina
Moscow Myasthenia Center
Email: fake@neicon.ru
Russian Federation
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